Secondary Metabolites from Dendrobium nobile and Their Activities Induce Metabolites Apoptosis in OSC-19 Cells

To identify potential drug candidates, secondary metabolites of Dendrobium nobile were performed. As a result, two previously undescribed phenanthrene derivatives with a spirolactone ring (1 and 2), along with four known compounds, N-trans-cinnamoyltyramine (3), N-trans-p-coumaroyltyramine (4), N-trans-feruloyltyramine (5), and moscatilin (6), were isolated from Dendrobium nobile. The structures of the undescribed compounds were elucidated using NMR spectroscopy, electronic circular dichroism (ECD) calculations, and extensive spectroscopic data analysis. The cytotoxic effects of compounds on human tongue squamous cells OSC-19 were determined using MTT at concentrations of 2.5 μM, 5 μM, 10 μM, and 20 μM. Compound 6 exhibited potent inhibitory activity against OSC-19 cells with an IC50 of 1.32 μM. Migration assays and western blot assays demonstrated that compound 6 effectively inhibited migration by down-regulating MMP2 and MMP9 at concentrations of 0.5 μM and 1 μM. To investigate its effect on apoptosis, we performed AO/PI staining, flow cytometry, and WB experiments. The results showed that increasing concentrations led to increased red fluorescence, decreased green fluorescence, increased apoptosis rate, decreased expression of bcl-2, caspase 3, caspase 9, and parp proteins, and increased bax expression. Furthermore, the phosphorylation of JNK and P38 was activated, suggesting that compound 6 may induce apoptosis via the MAPK pathway.


Introduction
Tongue cancer is a highly malignant tumor that occurs in the oral and maxillofacial region. It has the highest incidence rate among all oral cancers, accounting for approximately one-third of cases [1,2]. This type of cancer is characterized by rapid growth, strong infiltration, and high malignancy, which can result in impaired speech, mastication, and respiratory function, posing a significant threat to human health [3][4][5]. Searching for natural anticancer remedies with low toxicity and high efficacy has become a topic of great interest for researchers both at home and abroad. One such plant under investigation is Dendrobium nobile Lindl, a genus of the family orchidaceae, which is primarily distributed in China (specifically, Sichuan, Yunnan, Guizhou, Taiwan, Hu-bei, Guangdong, Hainan, and Guangxi provinces), and grows on trees in forest slopes and on rocks by the roadside at altitudes ranging from 800 to 1700 m above sea level. D. nobile has been used for thousands of years as a traditional Chinese herbal medicine and is also consumed as a food [6]. Previous studies have identified bibenzyls [7,8], sesquiterpenes [9][10][11], alkaloids [12,13], and phenanthrenes [8] as the primary components of D. nobile. Pharmacological research has revealed that D. nobile exhibits numerous health benefits, including immunomodulating, neuroprotective, hepatoprotective, anti-tumor, anti-oxidation, anti-diabetic, anti-platelet aggregation, and bacteriostasis activities. Previous studies have demonstrated that bibenzyls and their derivatives possess outstanding anti-tumor effects in vitro [14,15]. In our continued efforts to discover new and distinctive bioactive compounds from the Dendrobium genus, we have isolated two previously unknown phenanthrene derivatives featuring a spirolactone ring (1 and 2), along with four known compounds (3)(4)(5)(6), from D. nobile. The structures of these previously unknown compounds were determined using NMR spectroscopy, electronic circular dichroism (ECD) calculations, and extensive spectroscopic data analysis. We evaluated the cytotoxic effects of the isolated compounds on the OSC-19 human tongue squamous cell line using the MTT assay, finding that compound 6 showed excellent inhibitory activity against this cell line. Furthermore, we investigated its anticancer mechanism.

Isolation and Structure Elucidation
The dried D. nobile was refluxed with 90% methanol to obtain a crude extract. The EtOAc extract was separated by various column chromatographers to obtain compounds 1-6 ( Figure 1).  [14,15]. In our continued efforts to discover new and distinctive bioactive compounds from the Dendrobium genus, we have isolated two previously unknown phenanthrene derivatives featuring a spirolactone ring (1 and 2), along with four known compounds (3−6), from D. nobile. The structures of these previously unknown compounds were determined using NMR spectroscopy, electronic circular dichroism (ECD) calculations, and extensive spectroscopic data analysis. We evaluated the cytotoxic effects of the isolated compounds on the OSC-19 human tongue squamous cell line using the MTT assay, finding that compound 6 showed excellent inhibitory activity against this cell line. Furthermore, we investigated its anticancer mechanism.

Effect of Compounds on Proliferation Activity in OSC-19
In order to investigate the impact of various compounds on cellular proliferation in the OSC-19 cell line, an MTT assay was conducted at concentrations of 2.5 µM, 5 µM, 10 µM, and 20 µM. OSC-19 cells were exposed to varying concentrations of the compounds for 48 h. The results indicate that compounds 3, 4, and 5 exhibited insignificant inhibitory effects, whereas moscatilin demonstrated a dose-dependent inhibition of OSC-19 cell growth with a significant IC50 value of 1.32 µM (Figure 4).   Figures S8-S12) were similar to those of compound 1, which indicated that compound 1 was a homologue of compound 1. The 1 H NMR spectrum (Table 1) of compound 2 showed the presence of 10 aromatic proton signals, one signal more than compound 1. By comparing the 13 C NMR spectrum with those of compound 1, the chemical shift of C-9 was shifted to high-field (δ C 152.3 in 1, δ C 130.6 in 2). Similarly, the signals of C-10 (δ C 121.2), C-8a (δ C 134.3), and C-8 (δ C 112.5) were shifted (∆δ = +20.9, +6.1, and +5.6, respectively). These changes indicated that the proton at C-9 in compound 2 replacement of the hydroxyl group at C-9 in compound 1. The CD spectrum of compound 2 matched well with that of compound 1 and implied that the absolute configuration was R. In summary, the structure of compound 2 was determined and named dendnobione B.

Effect of Compounds on Proliferation Activity in OSC-19
In order to investigate the impact of various compounds on cellular proliferation in the OSC-19 cell line, an MTT assay was conducted at concentrations of 2.5 µM, 5 µM, 10 µM, and 20 µM. OSC-19 cells were exposed to varying concentrations of the compounds for 48 h. The results indicate that compounds 3, 4, and 5 exhibited insignificant inhibitory effects, whereas moscatilin demonstrated a dose-dependent inhibition of OSC-19 cell growth with a significant IC 50 value of 1.32 µM (Figure 4).

Moscatilin Inhibits the Migration of Tongue Cancer Cells
Epithelial mesenchymal transition (EMT) is the process by which epithelial cells undergo transformation into mesenchymal cells. This process involves the loss of original cell polarity, leading to the breakdown of tight junctions and adhesive links between cells, resulting in infiltrative and wandering migration abilities. In addition, the expression of mesenchymal marker proteins, such as MMPs and vimentin is upregulated. When OSC-19 cells were treated with moscatilin for 24 h, their migration was found to be inhibited in a dose-dependent manner (Figure 5a,b). Furthermore, western blot analysis revealed a decreased expression of MMP2 and MMP9 (Figure 5c,d). These results suggest that moscatilin may suppress EMT by reducing the expression of MMP2 and MMP9 proteins, thereby inhibiting the migration of tongue cancer cells.

Moscatilin Inhibits the Migration of Tongue Cancer Cells
Epithelial mesenchymal transition (EMT) is the process by which epithelial cells undergo transformation into mesenchymal cells. This process involves the loss of original cell polarity, leading to the breakdown of tight junctions and adhesive links between cells, resulting in infiltrative and wandering migration abilities. In addition, the expression of mesenchymal marker proteins, such as MMPs and vimentin is upregulated. When OSC-19 cells were treated with moscatilin for 24 h, their migration was found to be inhibited in a dose-dependent manner (Figure 5a,b). Furthermore, western blot analysis revealed a decreased expression of MMP2 and MMP9 (Figure 5c,d). These results suggest that moscatilin may suppress EMT by reducing the expression of MMP2 and MMP9 proteins, thereby inhibiting the migration of tongue cancer cells.  Figure 6 shows that the exposure of OSC-19 cells to moscatilin for 24 h resulted in chromatin shrinkage and condensation, reduced tumor-cell count, and increased red fluorescence in a dose-dependent manner (Figure 6a). Flow cytometry (FCM) analysis revealed that the apoptosis rate increased from 2.53 ± 0.28% and 5.63 ± 0.61% to 11.2 ± 1.92% after 24 h of incubation at 0.5 µM and 1 µM concentrations, respectively ( Figure  6b,c). Western blot assays detected increased expression of Bax, Cleaved Caspase 3, Cleaved Caspase 9, and Cleaved PARP after moscatilin treatment, while Bcl-2 expression was inhibited, confirming the occurrence of apoptosis (Figure 6d,e).  Figure 6 shows that the exposure of OSC-19 cells to moscatilin for 24 h resulted in chromatin shrinkage and condensation, reduced tumor-cell count, and increased red fluorescence in a dose-dependent manner (Figure 6a). Flow cytometry (FCM) analysis revealed that the apoptosis rate increased from 2.53 ± 0.28% and 5.63 ± 0.61% to 11.2 ± 1.92% after 24 h of incubation at 0.5 µM and 1 µM concentrations, respectively (Figure 6b,c). Western blot assays detected increased expression of Bax, Cleaved Caspase 3, Cleaved Caspase 9, and Cleaved PARP after moscatilin treatment, while Bcl-2 expression was inhibited, confirming the occurrence of apoptosis (Figure 6d,e).

Moscatilin Induces Apoptosis through MAPK Signaling Pathway
The results of the western blot assay showed that moscatilin, at different concentrations, significantly promoted the phosphorylation of ERK, JNK, and P38 MAPK compared with the control group (0 µM group), suggesting that moscatilin may induce apoptosis in OSC-19 cells by promoting the phosphorylation of ERK, JNK, and P38 MAPK (Figure 7).

Moscatilin Induces Apoptosis through MAPK Signaling Pathway
The results of the western blot assay showed that moscatilin, at different concentrations, significantly promoted the phosphorylation of ERK, JNK, and P38 MAPK compared with the control group (0 µM group), suggesting that moscatilin may induce apoptosis in OSC-19 cells by promoting the phosphorylation of ERK, JNK, and P38 MAPK (Figure 7).

Plant Material
Dendrobium nobile Lindl was harvested in Guizhou Province, China, in 2014 and identified as Dendrobium nobile Lindl by associate Prof. Yang Jian-Wen (Zunyi Medical University). A voucher specimen (No. 20141011) was deposited at the School of Pharmacy, Zunyi Medical University.

Extraction and Purification of Compounds 1-6
The dried D. nobile was crushed, then heated and refluxed with 90% methanol for extraction thrice, each time for 3 h. The methanol extract was evaporated under reduced pressure to obtain a crude extract, which was further suspended in water and extracted with EtOAc and n-BuOH (3 times each). EtOAc extract was subjected to silica gel column chromatography (70 mm × 660 mm, 300-400 mesh), elution with petroleum ether, EtOAc and methanol, and monitored using TLC to compile the resulted similar fractions. Based on TLC analysis, 12 fractions were further investigated. Fr

Cell Viability Assay
A cell viability assay was performed as described previously [22]. OSC-19 cells were plated on 96-well culture plates at a density of 3 × 10 3 cells per well. After 12 h, cells were treated with varying concentrations (2.5 µM, 5 µM, 10 µM, and 20 µM) of moscatilin for 48 h. After treatment, cells were incubated with MTT (5 mg/mL) for 4 h. Carefully remove the medium and add 150 µL of DMSO to each sample and shake for 30 min. The cell absorbance value (A value) at 490 nm was detected using a micro plate reader. The results were analyzed using GraphPad Prism 8 software.

Migration Assay
A migration assay was carried out as described previously [23]. The OSC-19 cells were cultured in a 6-well plate containing DMEM medium and 10% FBS. After confluence, wounds were performed in each well. Aspirate the supernatant, wash twice with PBS to remove cell debris, and add 1 mL of 0.5 µM and 1 µM moscatilin. Photos were taken using an inverted microscope at 0 h and 24 h, recording the scratch healing, and calculating the scratch healing area.

Apoptosis Assessment by AO/PI Staining
To determine the effect of moscatilin on OSC-19 cell viability, an AO/PI staining experiment was conducted [23]. OSC-19 cells were seeded into 24-well plates and incubated at 37 • C for 12 h. The cells were then treated with varying concentrations of moscatilin (0.5 µM and 1 µM) for 24 h. After removing the medium and washing twice with PBS, acridine orange (AO) and propidium iodide (PI) were added to the 24-well plate at a concentration of 100 µg/mL each and stained for 5 min at room temperature in the dark. Finally, the staining was observed using a fluorescence microscope. AO dye stains all nucleated cells, both live and dead, producing green fluorescence, while PI dye stains only dead nucleated cells, producing red fluorescence.

Annexin V-FITC/PI Assay for Apoptosis
The annexin-V FITC apoptosis detection kit was used to verify the moscatilin-induced cell death pattern using annexin-V FITC analysis [24]. Similarly, The OSC-19 cells were seeded into 6-well plates and treated with varying concentrations of moscatilin (0.5 µM and 1 µM) for 24 h, the samples were harvested. Then, 195 µL of annexinV-FITC binding buffer was used to resuspend the cells and stained with 10 µL PI and 5 µL annexin V-FITC for 15 min in the dark, and the apoptosis ratio was analyzed using flow cytometry. Each sample was measured in three separate replicate experiments.

Western Blot Analysis
Western blot analysis was performed as described previously [25]. OSC-19 cells were seeded into 6-well plates at a density of 4 × 10 5 cells/well and incubated with varying concentrations of moscatilin (0.5 µM and 1 µM). Then cells were lysed in radioimmunoprecipitation a pssay buffer (RIPA), and protein concentration was quantified using a BCA protein assay kit. For western blot, proteins were separated in 10% SDS polyacrylamide gels and transferred to PVDF membranes. After blocking with 5% fat-free milk for 60 min at room temperature, they were incubated with primary antibodies at 4 • C overnight. The membranes were then washed with TBST buffer and incubated with an HRP-conjugated secondary antibody at room temperature for 60 min. After several washes of TBST, the blots were developed using enhanced chemiluminescence (ECL) solution.

Statistical Analysis
Statistical analyses were performed by using the GraphPad Prism 8 package. All experiments were carried out in triplicate and the averages of the three independent experiments were used as the statistical result. The results were represented as the mean ± standard deviation (SD). A one-way analysis of variance (ANOVA) was conducted, followed by Dunnett's test compared with the control group. p ≤ 0.05 was considered statistically significant.

Conclusions
In summary, two new phenanthrene derivatives containing a spiro-lactone ring (1 and 2) and four known compounds (3)(4)(5)(6) were isolated from D. nobile. The MTT assay showed that moscatilin had better inhibitory activity against OSC-19 human tongue squamous cells, prompting further investigation of its anti-cancer mechanism. The results revealed that moscatilin induced apoptosis in OSC-19 cells by regulating Bcl-2 family proteins and caspase family proteins. In addition, treatment with moscatilin increased the phosphorylation of JNK MAPK and P38 MAPK. Furthermore, moscatilin inhibited OSC-19 cell migration by suppressing EMT through the downregulation of MMP2 and MMP9 activity.