1. Introduction
Metabolic reprogramming is an adaptation mechanism implemented by cancer cells in response to their microenvironment, which alters their metabolism to sustain the energy request for growth and proliferation [
1]. Usually, the tumor microenvironment is hypoxic, acidic, and low in nutrients; despite these conditions, the cells present an abnormal metabolism to maintain themselves and to keep growing, including alterations in the tricarboxylic acids (TCA) cycle, glycolysis, the urea cycle (UC), nitric oxide (NO) metabolism, polyamines biosynthesis, and protein, lipid, and nucleic acid biosynthesis [
2]. Today, one of the most important emergent therapies with remarkable potential is to modulate the metabolic reprogramming of cancer cells [
2].
L-Arginine plays a central axis due to its ability to be incorporated into the anabolic and catabolic pathways mentioned before. In non-cancer cells, L-arginine is usually derived from exogenous uptake from the diet and endogenous biosynthesis through UC intermediates [
3]. Once it has been absorbed, L-arginine can be incorporated into protein synthesis, acting as a building block. Moreover, L-arginine is reported to positively regulate anabolism itself by upregulating mTORC1 activity through the modulation of CASTOR1 and SLC38A9, the arginine sensors of the cells [
4]. In addition, L-arginine is the precursor of a plethora of substances needed for proliferation, immune system regulation, DNA repair, or regulation of gene expression, such as polyamines, NO, and creatine. L-Arginine is key in two polyamine-producing pathways: the first pathway is the decarboxylation of L-arginine to agmatine by arginine decarboxylase (ADC) and subsequent hydrolysis via agmatinase, culminating with putrescine production; the second pathway involves L-ornithine, which is derived from L-arginine hydrolysis via arginase (ARG) in the UC. In addition, L-arginine is also involved as a precursor in the nitric oxide synthase (NOS)-catalyzed NO production and in the protein arginine methyltransferase (PRMT)-dependent production of the dimethylated derivatives of L-arginine: asymmetric dimethylarginine (ADMA) and symmetric dimethylarginine (SDMA). There are three NOS isoforms: inducible (iNOS), endothelial (eNOS), and neural (nNOS); eNOS is involved in vascular tone regulation, but iNOS is normally overexpressed during inflammation. On the other hand, ADMA is considered to be a potent competitive inhibitor of NOS that leads to less NO production. In addition to this, in the kidneys, L-arginine serves as the precursor of guanidinoacetate (GAA) via arginine:glycine amidinotransferase (AGAT), which is transported to the liver and converted into creatine by guanidinoacetate N-methyltransferase (GAMT) [
3]. Interconversion between creatine and phosphocreatine in the cells in the so-called phosphagen system can maintain the different ATP pools by phosphorylating ADP to ATP via different isoforms of creatine kinases (CK), such as the muscle-type and brain-type CK [
5].
Cancer cells reprogram L-arginine metabolism to support the proliferation and progression of malignancy, suppressing the immune response, and regulating gene expression [
2]. The absorption of L-arginine in cancer cells is achieved by the overexpression of cationic amino acid transporters [
6]. Indeed, hyperactivation of mTORC1 by L-arginine sensors has been reported in several types of cancer and is associated with increased anabolic pathways, such as the biosynthesis of nucleotides, protein, and fatty acids, and with the suppression of autophagy [
7]. In tumors, UC was reported to be disrupted at different points. For instance, ORNT1, OTC, ASS1, and ASL were commonly downregulated. Additionally, it was observed at a higher carbamoyl phosphate concentration and its consequent input in the pyrimidine biosynthesis by carbamoyl phosphate synthetase 2 (CPS2) [
8]. These metabolic changes led to increases in cellular growth and survival. Additionally, increased polyamines concentrations are usually observed in cancer cells. Polyamines have been implicated in nucleic acids and protein synthesis, chromatin stabilization, the regulation of paracrine communication, and prevention against oxidative DNA damage [
9]. It has been reported that cancer cells exhibit increased ARG expression and activity, leading to a high production of L-ornithine [
10]. Some studies also reported the overexpression of ODC1 due to MYC activity with a subsequent elevation in the putrescine concentration [
11,
12]. These alterations contribute to cancer progression. Furthermore, cancer cells can restore energy by using the phosphagen system to allow increased proliferation and survival. Additionally, creatine plays a key role in immunity by modulating T cells and acting as an efficient energy buffering mechanism when the cells demand high levels of ATP due to the high phosphate transfer potential of phosphocreatine [
13,
14]. Although some studies have showed contradictory results about expression of CK isoforms, CK has been correlated with the cancer prognosis [
14,
15,
16]. Regarding NO metabolism, it was reported that NO had a paradoxical dual activity, i.e., it promoted several hallmarks of cancer, such as apoptosis inhibition, epithelial-to-mesenchymal transition induction, and increased vascular infiltration and permeability, but at the same time, it was reported that NO counteracts the mechanisms mentioned before [
17]. Further, decreased ADMA levels were reported in prostate cancer due to the upregulation of ADMA breakdown via dimethylarginine dimethylaminohydrolase (DDAH), leading to high NOS activity and angiogenesis [
18].
Taking advantage of L-arginine dependency in some tumors, in arginine deprivation therapy (ADT), L-arginine levels are decreased by administering arginine-depleting agents, such as pegylated arginine deiminase or pegylated arginase 1 [
19]. ADT has shown promising results due to the pivotal role of L-arginine and their related metabolites involved in cancer metabolism, e.g., NO, ADMA, polyamines, and creatine, although cancer sensitivity seems to be dependent on the urea cycle enzymes [
19,
20]. Hence, the modulation of metabolic reprogramming by deprivation therapies or other approaches seems a rational alternative to some specific cancer types, and more research is needed to improve its efficacy and application.
In pharmacology, the disruption of specific metabolic pathways has been performed using structurally related molecules that resemble endogenous ligands. For instance, statins imitate the structure of β-hydroxy-β-methylglutaryl-CoA (HMG-CoA), leading to the inhibition of HMG-CoA reductase and blocking cholesterol biosynthesis [
21]. In line with this, there are several reports about metformin altering different metabolites related to L-arginine, suggesting the potential to interfere with UC, creatine biosynthesis, NO production, and polyamines metabolism [
22].
Metformin, buformin, and phenformin are biguanides with anti-diabetic properties but nowadays, metformin is the only biguanide on the market and the first-line treatment for management of type 2 diabetes mellitus. Beyond their anti-diabetic properties, anticancer effects have been described in both in vitro and in vivo assays [
23]. Despite it being such a versatile drug, the mechanism (or mechanisms) of action behind these effects remain elusive. Currently, the most established anti-cancer mechanism of action is the activation of AMP-activated protein kinase (AMPK) due to the energy deficit induced by the metformin-dependent inhibition of mitochondrial complex 1. In turn, AMPK activation negatively regulates those energy-consuming metabolic pathways, e.g., gluconeogenesis, glycogen synthesis, and fatty acid synthesis, but upregulates energy-generating metabolic pathways, e.g., glycolysis, glycogen breakdown, fatty acid oxidation, and autophagy [
24].
However, there are some inconsistencies about this previous description related to the simplicity of metformin’s chemical structure. With a small structure and the lack of directing groups compared to other complex drugs, it is virtually impossible that metformin could bind to only one target in the cell. Even the more complex drugs usually act through binding to different targets [
25]. Molecular promiscuity appears to be a more logical approach to understand metformin’s anti-cancer mechanism of action. Given that the basic metformin’s pharmacophore is the guanidine group, it is reasonable to think that it may resemble guanidine-containing endogenous ligands inside the cell, e.g., L-arginine, creatine, ADMA, or some other related metabolites (
Figure 1). Our hypothesis states that metformin (and biguanides in general) may be acting in the cancer cell as an antagonist of L-arginine and its related metabolites, leading to modulation of their corresponding targets, and, therefore, altering the metabolic reprogramming of cancer cells.
Computational tools can be employed to generate, transform, interpret, predict, and visualize data of a chemical and biological nature. These tools are commonly applied in drug discovery and exploration of the biological effects of molecules, allowing the prediction of physicochemical properties and drug-likeness, or even the prediction of possible targets according to the ligand structure [
26]. In bioinformatics, molecular dynamics and molecular docking are commonly used to model the binding of ligands to specific targets, and to predict the affinities of ligands to targets of interest. However, molecular docking is normally used as a quick and inexpensive exploratory tool to generate preliminary insights to design further experiments [
27]. On the other hand, given the computational power needed to run molecular dynamics simulations and the long waiting times needed to perform the thermodynamic calculations, it has been used as a more reliable computational technique to further validate the interactions observed in molecular docking simulations or experimental evidence [
26]. In addition, it is common to use machine learning algorithms to extract relevant and significant information from the data [
28]. In general, computational tools have demonstrated a high potential to generate, develop, and sustain hypotheses, as well as, to gain insights about the molecular actions of substances, as a first step before experiment design and performance [
26]. For instance, exploration of the possible mechanism of action behind the arrest of the cell cycle in the sub-G1 phase in cancer cells led to the identification of possible interactions of geranyl farnesol, sahandinone, and 4-dehydrosalvilimbinol, a group of terpenoids present in
Salvia lachnocalyx, with DNA topoisomerase I through a computational methodology centered on molecular docking and molecular dynamics simulations, suggesting that these terpenoids could be good candidates for the design of new drugs [
29]. On the other hand, it has been reported that six possible targets genes (e.g., AR, HSP90AA1, MMP9, PGR, PTGS2, and TNF) are responsible for the action of the pseudo phosphorous stem of
Cremastra appendiculata by employing a reverse network pharmacology approach that can allow for the in vitro or in vivo targeted study of molecular actions in the future [
30]. The computational methodology they followed included tools for predicting the physicochemical properties and biological targets, such as SwissADME and SwissTargetPrediction, respectively, as well as tools to predict the binding and affinity of ligands in different targets of interest, such as molecular docking [
30].
To test this hypothesis, in the present work, we employed different cheminformatic tools to seek for structural and physicochemical similarities between biguanides and different L-arginine-related metabolites by employing tools, such as the PubChem Score Matrix Service, SwissADME, and SwissTargetPrediction. Finally, we employed molecular docking, a bioinformatic technique, to test if the chemical similarity observed for biguanides may be translated into similar binding modes and affinities to those of L-arginine-related metabolites in their corresponding targets. Given that the complete metformin’s mechanism of action is still unknown, the relevance behind our hypothesis and this study is the establishment and support of a new possible theoretical framework to progress in the understanding of metformin’s biological actions in cancer cells, although this knowledge may be extrapolated to improve the comprehension of its therapeutic effects in other diseases where L-arginine, or its related metabolites, play a pivotal role.
2. Results
2.1. Database Creation
Before performing the different comparisons, we created a database containing the candidate metabolites, whose simplified molecular-input line-entry system (SMILES) and their compound ID (CID) were collected from PubChem. There were 20 candidate molecules in the final version of the constructed database, including 3 biguanides (metformin, buformin, and phenformin), 7 members of the UC (L-ornithine, L-citrulline, carbamoyl phosphate, L-aspartic acid, L-argininosuccinic acid, fumaric acid, and urea), L-arginine and their endogenous methylated derivatives (ADMA and SDMA), 5 members from the polyamine metabolism (agmatine, putrescine, spermine, spermidine, and cadaverine), and 2 members from creatine biosynthesis (guanidinoacetic acid and creatine).
2.2. Structural Comparison between Biguanides and L-arginine-Related Metabolites
After generating the database, we proceeded to assess the structural similarity between biguanides and the candidate metabolites by employing the PubChem Score Matrix Service to compare their chemical structures at two levels: the 2D level and 3D level. Selected results about the comparison of biguanides against candidate metabolites are shown in
Table 1 for the 2D and 3D analyses, while the complete results can be observed in the
Supplementary Material.
Tanimoto coefficients (TC) were generated from 2D structural comparisons. They ranged from 0 to 100 depending on the grade of the 2D structural similarity. The higher the TC value is, the more structurally similar the compared molecules are. Given metformin, buformin, and phenformin share the same pharmacophore, we expected to see high TC values (TC ≥ 65) between them. However, as shown in
Table 1, a moderate similarity was observed only between metformin and buformin with a TC of 63, while phenformin showed low similarities with metformin (TC of 23) and buformin (TC of 33). Compared to those of the candidate metabolites, there were moderate similarities observed for buformin against different polyamines, e.g., cadaverine, spermidine, spermine, and putrescine, with TC values ranging from 51 to 62. It is noteworthy that buformin showed a high similarity with agmatine (TC of 88), but a moderate similarity against guanidinoacetic acid (TC of 50), an intermediate of creatine biosynthesis. On the other hand, metformin showed moderate similarity only with agmatine (TC of 56), and phenformin did not even reach or surpass a TC of 50 with any candidate metabolite.
Related to TC, Shape Tanimoto (ST) and Color Tanimoto (CT) were generated from 3D structural comparisons. They ranged from 0 to 100 depending on the grade of similarity in terms of shape or features (H-bonding donors or acceptors, rings, etc.), respectively. When ST and CT were summed up, combo T was generated, and it describes both the shape and features in only one parameter going from 0 to 200. Similar to the 2D structural comparisons, at the 3D level, the results suggested a moderate similarity between metformin and buformin with a combo T of 122, but phenformin still showed a low level of similarity with metformin (combo T of 89). Additionally, when phenformin was compared with buformin at the 3D level, its similarity was moderate (combo T of 111). Compared to the candidate metabolites, metformin showed moderate similarities against L-arginine, cadaverine, creatine, agmatine, and L-ornithine with combo T values going from 101 to 129. It is noteworthy that metformin showed higher similarities compared to those of guanidinoacetic acid and L-aspartic acid (combo T > 130). In the same way, buformin showed moderate similarities against L-arginine, agmatine, guanidinoacetic acid, creatine, and spermidine, with combo T values ranging from 102 to 120. Only phenformin showed lower similarities (combo T < 100) compared to those of all the candidate metabolites.
Remarkably, the moderate-to-high similarity observed for metformin or buformin compared to those of some candidate metabolites was due principally to their high level of shape resemblance with ST values > 80. On the other hand, the CT values tended to be less than 50 because of the high diversity of functional features of tested metabolites. However, the presence of the common guanidine moiety in L-arginine, agmatine, creatine, and guanidinoacetic acid led to the highest CT values observed for biguanides.
Finally, we performed another structural similarity assay employing the SwissSimilarity tool, aiming to reproduce the previous observations by seeking if there were a common scaffold between the biguanides and some candidate metabolites. As we anticipated in our hypothesis, the results showed that L-arginine, agmatine, creatine, spermidine, and cadaverine shared a common scaffold with metformin and buformin, but not phenformin (data not shown).
Considering only structural criteria, these results suggested moderate-to-high structural similarities between the biguanides, especially metformin and buformin, and some candidate metabolites, such as agmatine, intermediates from UC and, especially, creatine biosynthesis.
2.3. Physicochemical Comparison between Biguanides and L-arginine-Related Metabolites
The physicochemical comparisons between biguanides and the candidate metabolites began with the prediction of their physicochemical properties, employing the collected SMILES through the SwissADME tool [
31]. The predictions were performed in ionized (pH 7.4) and non-ionized modalities. For each molecule, we collected seven physicochemical parameters, including molecular weight, consensus log P, topological polar surface area (TPSA), rotatable bonds, the number of hydrogen bond donors and acceptors, and the fraction of sp
3 carbons. After the results were collected for each modality, the analysis of those parameters aiming to obtain the similarity under physicochemical criteria was performed. To identify physicochemical relationships between biguanides and the candidate metabolites, an unsupervised machine learning approach with the collected results was employed. First, we performed a principal component analysis (PCA), employing our variables as an exploratory analysis of the data. The PCA of ionized modality showed a close relationship of metformin and buformin with creatine, guanidinoacetate, and L-aspartate. In terms of the physicochemical properties, phenformin was isolated in the PCA. When it was performed in the non-ionized modality, the PCA showed that all the biguanides were similar to creatine, agmatine and L-ornithine in terms of physicochemical properties.
After that, we proceeded to perform hierarchical clustering (HC) using the different physicochemical profiles. First, preliminary hierarchical clustering including only candidate metabolites was performed. After that, each biguanide was compared, one at a time, against the different candidate metabolites in HC.
Without including any of the biguanides, the preliminary hierarchical clustering at both the ionized and non-ionized modalities generated a cluster for L-arginine, L-citrulline, ADMA, and SDMA, metabolites that belong to the urea cycle and NO metabolism. Polyamines were grouped in two clusters: one for low-molecular-weight polyamines (putrescine and cadaverine) and high-molecular-weight polyamines (spermidine and spermine). In the case of ionized modality, L-ornithine was grouped together with spermidine and spermine. With some differences, creatine, agmatine, guanidinoacetic acid, and L-aspartic acid were grouped together at both of the modalities, accounting for metabolites from the urea cycle, polyamines metabolism, and, mainly, creatine metabolism. L-Argininosuccinic acid alone and fumaric acid with urea (and carbamoyl phosphate in the ionized modality) are represented in the last two clusters.
When metformin was included in the HC, this was grouped together with creatine, guanidinoacetic acid, and L-aspartic acid in both modalities, although in the non-ionized modality, L-ornithine and agmatine were also included (
Figure 2). In the case of buformin, this was grouped together with agmatine, creatine, guanidinoacetic acid, and L-aspartic acid, although in the non-ionized modality, L-ornithine and carbamoyl phosphate were also included. Finally, phenformin was grouped with fumaric acid and urea, but carbamoyl phosphate was included in the ionized modality.
As can be observed, the physicochemical comparison agreed with the previous structural relationships obtained for metformin and buformin against creatine, guanidinoacetate, agmatine, and L-aspartate. Although phenformin showed a physicochemical relationship with agmatine, creatine, and L-ornithine during the PCA in the non-ionized modality, physiologically, non-ionized relationships are of little relevance because all the candidate metabolites and biguanides are ionized inside the cell. This is observed when the PCA was performed in the ionized modality, where phenformin was alone. PCA analyses and all the hierarchical clustering are shown in the
Supplementary Material.
By limiting our analysis to both structural and physicochemical criteria, these results suggested a relationship between metformin and buformin, but not phenformin, with agmatine, L-aspartate, and especially, intermediates from creatine metabolism.
2.4. Structure-Based Target Prediction of Biguanides and L-arginine-Related Metabolites
Once we observed structural and physicochemical similarities of biguanides with some arginine-related metabolites, we were interested in testing if this similarity could be translated into an affinity for targets whose main substrates or ligands belong to the candidate metabolites included in the database that we tested before. To prove this assumption, we performed a structure-based target prediction employing the SwissTargetPrediction tool [
32]. For each predicted target, its probability score, and its known actives 3D/2D were collected. We observed that biguanides, especially phenformin, were predicted to target the three different isoforms of nitric oxide synthase, whose main substrate is L-arginine, and its main inhibitor is ADMA. However, only the neural isoform of NOS was predicted with a high probability score, although the known actives 3D/2D parameter suggested all biguanides could target the inducible, endothelial, and neural isoforms. Furthermore, the known actives 3D/2D suggested that biguanides could also bind to several isoforms of carbonic anhydrases, whose known ligands are polyamines.
Indeed, these observations agree with our previous results of structural and physicochemical similarities that showed moderate-to-high similarities of biguanides to intermediates from polyamines metabolism, NO production, and UC. The complete predicted targets for biguanides can be found in the
Supplementary Material.
2.5. Affinity Comparison between Biguanides and L-arginine-Related Metabolites
Following the target prediction in the SwissTargetPrediction tool, we proceeded to perform a molecular docking simulation to test if the affinities were comparable to those of candidate metabolites in their corresponding targets. The protein files required for the simulation were obtained from Protein Data Bank [
33]. All the sites employed in the simulation were based on information from UniProt and predictions from the DoGSiteScorer tool [
34,
35].
The results from the molecular docking simulations are shown in
Figure 3. In general, there was a trend for metformin, buformin and phenformin, in that order, of being the biguanides with the highest affinities to each target. Additionally, according to binding energies and predicted inhibition constants, phenformin showed even more affinity than the endogenous ligands did during their binding to some targets. For instance, the binding energies for metformin (−8.09 kcal/mol), buformin (−9.39 kcal/mol), and phenformin (−9.72 kcal/mol) in ARG1 were comparable to that obtained for L-arginine (−9.56 kcal/mol). Another example was CASTOR1, one of the L-arginine sensors in the cell, in which the binding energy for L-arginine was −9.3 kcal/mol, but in the case of metformin, buformin, and phenformin, they were −7.21 kcal/mol, −7.92 kcal/mol, and −10.34 kcal/mol, respectively. In the case of GAMT, biguanides showed comparable or even higher affinities (−6.9 kcal/mol to −9.48 kcal/mol) than guanidinoacetate did (−5.59 kcal/mol), the precursor of creatine. Furthermore, the binding energies of biguanides (from −7.76 kcal/mol to −9.9 kcal/mol) were similar to that of putrescine (−8.44 kcal/mol) in spermidine synthase. Finally, for the three isoforms of NOS, the estimated binding energies of biguanides ranged from −4.37 kcal/mol to −6.56 kcal/mol, while for L-arginine and ADMA, they ranged from −5.01 kcal/mol to −5.51 kcal/mol and from −5.07 kcal/mol to −5.42 kcal/mol, respectively. Remarkably, these results agreed with phenformin and metformin being the most and least potent biguanides, respectively [
36].
2.6. Binding Comparison between Biguanides and L-arginine-Related Metabolites
Despite the similarity between the predicted binding energies of biguanides and the candidate metabolites, we proceeded to assess the binding modes inside the tested targets to sustain our hypothesis about a structure-dependent cross mechanism of action. The different binding mode analyses were carried out in Chimera X 1.2.5. It is noteworthy that some biguanides’ binding modes were similar to those of candidate metabolites in their corresponding targets as shown in
Figure 4 for ARG1, CASTOR1, and brain-type CK. Other interactions can be found in the
Supplementary Material. We observed the establishment of hydrogen bonds between L-arginine and Asp 128, Asn 130, Ser 137, Thr 246, and Asp 232 in ARG1. Our simulation for the L-arginine binding mode in ARG1 agreed with the binding site reported in UniProt, which includes His 126, Thr 127, Asp 128, Ile 129, Asn 130, Ser 137, Gly 138, Asn 139, Asp 183, Thr 246, and Glu 277, indicating the good reproducibility of our methodology [
34]. Although with some differences, biguanides established hydrogen bonds with amino acid residues present in the L-arginine binding site, including Asp 128, Thr 246, and Glu 277, among others. As well as for ARG1, in CASTOR1, our simulation for L-arginine showed good reproducibility compared to that of the reported interacting amino acid residues from UniProt [
34]. In our methodology, L-arginine established hydrogen bonds with Val 112, Gly 274, Val 281, Thr 300, Phe 301, and Asp 304. With some differences, the biguanides shared interactions with different L-arginine-interacting amino acid residues, including Gly 274, Thr 300, Phe 301, and Asp 304. Finally, for the brain-type CK, the reported interacting amino acid residues in UniProt include Val 72, Glu 232, and Se 285 [
34]. Our simulation for creatine predicted the binding of the guanidine moiety to Glu 231 and Glu 232 and the carboxylate moiety to Arg 132 and Arg 292. Such as creatine, the guanidine moiety of biguanides showed a tendency to establish hydrogen bonds with Glu 231 and Glu 232, except for buformin, which established two hydrogen bonds with Arg 236 instead of Glu 232. Remarkably, the orientations of the guanidine groups inside ARG1, CASTOR1, and brain-type CK for L-arginine and biguanides were strongly similar.
As can be observed, these results are in line with our previous observations, where it should be expected to observe a good concordance of binding if the molecules are supposed to be similar.
3. Discussion
Beyond its anti-diabetic properties, metformin has showed to exert anti-cancer effects in different types of cancer models and epidemiological studies [
23]. Despite its clinical success and the progress made to elucidate its anticancer molecular actions, a complete picture of metformin’s anticancer biological effects is lacking. However, based only on structural and physicochemical characteristics, here, we proposed and sustained, with a computational methodology, our hypothesis that described another possible mechanism by which biguanides may resemble different endogenous L-arginine-related metabolites, leading to an antagonist effect in their corresponding targets.
In pharmacology, the binding of ligands to a specific target is dependent on several factors such as shape, charges, hydrogen-bonding capacity, flexibility, planarity, polarity, and size, among others [
37]. According to our hypothesis, if biguanides are supposed to bind targets from arginine-related metabolites, they must be comparable at both the structural and physicochemical levels. For this reason, the methodology followed here began with the creation of a database that contains different metabolites related to L-arginine metabolism and other related metabolic pathways including the urea cycle, nitric oxide, polyamines, and creatine metabolism. Subsequently, comparisons of the structural and physicochemical elements by employing cheminformatic tools were performed. In the final step to test our hypothesis, bioinformatic tools were carried out to prove if the comparable structural and physicochemical elements between biguanides and arginine-related metabolites could be translated into a comparable binding in their corresponding targets. If this was true, it is reasonable to think that biguanides may exert an anticancer effect by affecting the metabolic pathways where these metabolites are involved. In the following paragraphs, evidence that sustains or refutes our hypothesis is provided. However, the evidence is focused on metformin mainly because it is the most widely studied biguanide.
Anabolism supports proliferation, survival, and invasion processes in cancer cells. mTORC1 is one of the most important master regulators of anabolic metabolism in normal and cancer cells [
38]. The upregulation of mTORC1 has been reported to be dependent on two interrelated stimuli: proliferative signaling pathways by growth factors and nutrient sensing pathways by L-arginine, L-glutamine, and branched-chain amino acids [
4]. In cancer cells, anabolism dependency on L-arginine via mTORC1 has been associated with the activation of the RAGULATOR-RAG complex in the lysosomal membrane by both SLC38A9 and CASTOR1, the two intracellular sensors of L-arginine. SLC38A9 is a transmembrane transporter of L-leucine and L-arginine located on the lysosome that activates the RAGULATOR-RAG complex in response to changes in amino acids concentrations [
39]. The sensing of an amino acid via SLC38A9 has been reported to be needed in pancreatic cancer cells to form tumors [
40]. On the other hand, the binding of L-arginine to CASTOR1 disrupts its suppressing interaction with GATOR2, leading to the GATOR2-dependent inhibition of GATOR1 and the activation of the RAGULATOR-RAG complex [
41]. The CASTOR1-dependent inhibition of mTORC1 has shown a tumor suppressor role in lung adenocarcinoma leading to lower proliferation, migration, and invasion, and when it is downregulated, it is associated with a poor prognosis [
42]. It has been reported that the inhibition of mTORC1 through competitive binding in CASTOR1 by analogs of L-arginine, including L-citrulline and L-ornithine, among others, avoids the disruption of CASTOR1–GATOR2 interaction [
43]. Our hypothesis predicted that it may be possible the suppression of mTORC1 by the competitive binding of biguanides against L-arginine in CASTOR1 and SLC38A9, leading to decreased activity of the RAGULATOR-RAG complex and the consequent modulation of mTORC1. According to our results, metformin and buformin showed moderate structural similarities with L-arginine and L-ornithine, two reported ligands of CASTOR1. In addition, metformin and buformin are similar to L-ornithine in terms of the physicochemical properties. Additionally, the affinities and binding modes of all the biguanides were comparable or even higher than those obtained for L-arginine in CASTOR1 and SLC38A9. In agreement with our hypothesis and results, the inhibition of mTORC1 by a metformin treatment has been reported, independently of AMPK and TSC1/2, and in a RAG GTPase-dependent manner [
44]. Recently, it has been reported that L-arginine exerts an epigenetic regulation over TEA-like domain 4 (TEAD4) in prostate cancer cells [
45]. TEAD4 is a transcription factor that controls the expression of genes involved in oxidative phosphorylation. This suggests that global metabolism and epigenetics can be controlled by L-arginine in cancer cells via different sensing systems, such as CASTOR1, SLC38A9, and possibly TEAD4. As our hypothesis predicted, there was reported the metformin targeting of the YAP1–TEAD4 axis in bladder cancer cells [
46].
The urea cycle is related to several metabolic pathways that allow anabolism. For instance, the urea cycle was reported to be linked to the TCA via fumarate and oxalacetate-derived L-aspartate [
47]. Given this connection, the urea cycle disruptions were reported to modify TCA metabolites, leading to the metabolic and epigenetic changes needed for cancer cells. It is noteworthy that some essential building blocks and epimetabolites are directly derived from TCA, such as α-ketoglutarate [
48]. For instance, it has been reported that the fumarate accumulation in cancer cells allowed epithelial-to-mesenchymal transition due to the inhibition of the α-ketoglutarate-dependent dioxygenases, proteins with histone demethylase activity [
49]. Our results may indicate a possible reduction of urea cycle metabolites after the metformin treatment due to a cross structure-dependent inhibition of key enzymes. According to our analyses, metformin and buformin showed moderate-to-high similarities when they were compared at both the structural and physicochemical levels with some urea cycle metabolites, including L-aspartic acid, L-arginine, and L-ornithine. As expected, the structural and physicochemical similarities were translated in comparable affinities and binding modes of biguanides with urea cycle enzymes, at least in ARG1 and ARG2. Similar to this study, Detroja and Samson (2022) reported the possible inhibition of ARG1 by metformin based on molecular docking simulations and molecular dynamics. They found that the binding of metformin to the active sites of both ARG1 and ARG2 was stable for up to 50 ns in molecular dynamics simulations [
50]. There is evidence of biguanides affecting the urea cycle. According to Zhang et al. (2021), metformin has been shown to negatively regulate the urea cycle intermediates including L-arginine and L-aspartate in an in vivo xenograft model of HCT116, a colorectal cancer cell line [
51]. However, the authors reported that this reduction was due to the decreased expression in urea cycle enzymes such as CPS1, ARG1, and OTC. Additionally, it has been reported that the metformin treatment decreased the ARG1 activity of granulocytic myeloid-derived suppressor cells in a tumor-bearing mouse model of colon carcinoma [
52]. Furthermore, the decreased arginase activity was maintained despite the use of compound C, an AMPK inhibitor, suggesting that the reduction of arginase activity was independent on AMPK. In the same way, Koroglu-Aydin et al. (2021) reported a decreased activity of arginase in kidney homogenates from rats with diabetes and prostate cancer treated with metformin compared to that of non-treated rats [
53].
When they are altered, polyamines in cancer have been associated with increased proliferation, survival, and resistance to therapy, i.e., a poor cancer prognostic. In the case of polyamine metabolism, our results strongly supported the resemblance between biguanides and some specific intermediates. There was a remarkable structural similarity between buformin and metformin with agmatine and L-ornithine. These relationships were maintained during the physicochemical comparisons, although not in both modalities. As well as for the UC, metformin was capable of decreasing the concentrations of putrescine via decreased expression of ODC in an in vivo xenograft model of HCT116 [
51].
Cell division is a high-energy-demanding process that needs to be supported by plenty of energy. In cancer cells, a reported strategy to maintain the cell cycle forward was the overexpression of creatine kinases isoforms, especially in those sites where a lot of energy is needed [
54]. For these reasons, the phosphagen system represents one of the most important ways of storing, buffering, and transferring energy in tumors. Regarding creatine metabolism, our data indicated a competitive binding of biguanides against targets related to creatine biosynthesis or usage and the consequent disruption of cell bioenergetics. Our results showed moderate-to-high similarity at both the 2D and, especially, 3D levels. Additionally, the hierarchical clustering of biguanides with guanidinoacetic acid and creatine suggested a close relationship in terms of the physicochemical properties. On the other hand, the affinities and, for some isoforms of creatine kinases, the binding modes of biguanides were comparable to those obtained for creatine. It is noteworthy that metabolites belonging to creatine metabolism were the ones most related to biguanides, especially metformin and buformin, according to our results during structural, physicochemical, and binding comparisons. Recently, has authors have reported the competitive inhibition of AGAT by a metformin treatment (3 × 1500 mg daily for 6 weeks) in individuals with Becker muscular dystrophy, leading to reduced concentrations of guanidinoacetic acid in both serum and urine [
55]. Remarkably, decreased renal and pancreatic AGAT activity, but not decreased mRNA expression, have been reported after creatine supplementation in rats, suggesting that creatine can be involved in a negative feedback regulation mechanism [
56]. If biguanides were comparable to creatine, it may be possible that biguanides could become involved in that regulation, resembling creatine. Regarding the evidence supporting the action of biguanides on phosphocreatine biosynthesis, Garbati et al. (2017) reported the decrement of 40% in brain-type creatine kinase activity by metformin treatment (10 mM) during enzymatic assays, and its lowering effect on the ATP/AMP ratio of the KM-H2, SHSY-5Y, and MDA-MB-468 cancer cell lines [
57]. It is noteworthy that metformin was suggested to bind to a site different from that for creatine binding, acting in a non-competitive manner. It is possible that metformin may bind to the other isoforms of creatine kinases given the strong homology of this family of proteins [
58].
It is noteworthy that our main limitation was that our results were generated through a computational methodology. Hence, the experimental demonstration is needed to sustain or refute the results presented here and to test our hypothesis. Another limitation of our computational methodology was the absence of molecular dynamics simulations to test the binding of biguanides and L-arginine-related metabolites to the targets of interest in a more reliable manner, since both the protein and the ligand are flexible [
59]. However, the use of molecular dynamics simulations was beyond the scope of our original methodology, as our principal aim was to establish our hypothesis and to provide preliminary computational evidence about the possible structural, physicochemical, and binding similarities that biguanides share with some L-arginine-related metabolites, as a first approach. In the future, molecular dynamics simulations are intended to be included with an experimental methodology to provide stronger evidence for or against our hypothesis. Additionally, as mentioned above, authors have already reported the molecular dynamics simulations of metformin’s binding to ARG1/2, partially strengthening our molecular docking simulations results for metformin in the same targets [
50]. Another opportunity for improvement in the future is that in the present study, we limited our computational analysis to certain L-arginine-related metabolites, but there are many metabolites that may also be related structurally and functionally to biguanides, such as N(G)-monomethyl-L-arginine, L-proline, L-glutamate, or L-homoarginine, as well as different biguanides, including galegine or even microbiome-derived metabolites of biguanides.