Transcription in both sense and antisense directions has been reported, not only for regular genes, but also for those genes that are imprinted. In the same imprinted loci of H19, several antisense transcripts have been reported. A transcript that is antisense to IGF2, IGF2-antisense (IGF2-AS), is transcribed from within IGF2 in a reverse orientation. This transcript is also maternally imprinted [7]. LIT1 is an antisense transcript that is normally expressed from the paternal allele and lies within the KvLQT1 gene, and loss of imprinting (LOI) of LIT1 is linked to abnormal methylation of a differentially methylated region (DMR) upstream from the gene [8,9]. Those are not the only examples. Antisense transcripts have also been described for the imprinted genes, UBE3A, Zfp127/ZFP127, GNAS1 and IGF2R, to list some examples.

The H19 locus also produces antisense transcripts. Two such transcripts have been reported. Antisense to the H19 gene, the human H19 locus, encodes a translated product, called HOTS, for H19 opposite tumor suppressor [2]. A long antisense transcript, named 91H RNA, was also reported for both the human and the mouse H19/IGF2 loci [3].

Further characterization of HOTS indicated that it is an imprinted transcript, with the maternal allele actively expressed. HOTS transcript extends 1 kb upstream and 2.8 kb downstream of the H19 gene, comprising an approximate 6 kb polyadenylated transcript and containing a CpG island promoter [2].

The HOTS transcript is associated with the polysomes, suggesting its translation. The longest open reading frame (ORF) contained in HOTS that reside entirely on the H19 transcriptional unit encodes a predicted polypeptide of 150 amino acids that is well-conserved in primates, but not in the mouse, which has no ORF. A polyclonal antibody raised against HOTS detects HOTS in fetal tissues in monomeric and dimeric states and also in differentially expressed isoforms. Furthermore, HOTS has a putative nuclear localization signal and resides in the nucleus and the nucleolus, where it co-localizes with nucleophosmin [2].

Regarding the function of HOTS, data support a tumor suppressor activity. Using both overexpression and knockdown approaches, potent growth inhibition in vitro was observed and also a decrease in the ability of these cells to form colonies in soft agar. Furthermore, the in vivo tumorigenic potential of those cells was significantly impaired [2].

However, functioning as a tumor suppressor should at least indicate a possible mutation or downregulation of HOTS in cancer patients. To answer this question, Onyango et al. tried to identify mutations within the coding region of HOTS in samples of Wilm’s tumors. No such mutations were detected. However, analyses of a few cases of Wilm’s tumor with loss of heterozygosity (LOH) at 11p15 showed loss of HOTS expression [2]. It is clear that further work will be needed to understand the complex regulation of HOTS and H19 expression and the interrelationship between them and within the imprinted cluster as a whole.

A novel long intergenic 120-kb transcript antisense to the H19 gene has been identified at both the human and the mouse H19/IGF2 imprinted loci and is called 91H. The 91H RNA is short lived and almost exclusively nuclear, contrary to H19, which has equal distribution in the cytoplasm and the nucleus. In humans, the 5′ limit is located within intron 1 of the MRPL23 gene, located about 40 kb downstream of H19, and the 3′ limit is located about 70 kb upstream of H19. Thus, its promoter lies in an intron of an active host mRNA gene (MRPL23) [3].

Furthermore, it was shown that 91H was strongly and systematically over-expressed in breast cancer compared to normal breast tissues. The 91H RNA accumulation in breast cancer cells likely results from transcript stabilization. Like H19, the 91H RNA is also monoallelically expressed from the maternal allele [3].

The expression of 91H is very similar to H19, being dependent on the developmental stage in its regulation. It is also induced by the process of myoblastic cell differentiation, which may indicate that both H19 and 91H are sharing common regulatory schemes, which allow gene transcription in a time-restricted manner.

The functional role of 91H is addressed using RNAI technology. Although 91H silencing does not modify H19 imprinting status and has a minimal effect on H19 expression, it strongly reduces IGF2 mRNA levels.

It is not clear yet if HOTS forms a part of 91H.

One way by which ncRNA may acquire a function is by being a precursor of microRNA, which is capable of performing a regulatory function. Indeed, produced from exon 1 of H19, a miRNA-containing hairpin serves as a template for two distinct miRNAs, miR-675-5p and miR-675-3p[1]. Both, the full length H19 RNA and its miRNA have been identified also in marsupials. The stem loop region within H19 RNA is a highly conserved feature of the H19 RNA, clearly demonstrating that selective pressure may be higher on the miRNAs region than on H19 as a whole during mammalian evolution [10]. Apart from imprinting regulation, this important finding indicates that H19 may also control gene expression by post-transcriptional mechanisms. Whether H19 and its miR-675 have distinct functions or whether H19 functions through its miR-675 remains to be elucidated.

Recently, it was observed that no coordinated expression of H19 and miR-675 could be elucidated in tissues that are known to express a high level of H19 RNA during all stages of embryonic development, including the liver, while expressing only low levels of miR-675. This suggests the existence of an inhibitory mechanism hindering the processing of miR-675 from H19 RNA. However, in the placenta, maternal miR-675 expression is detected with increasing abundance from E11.5 till term [11].

Using a variety of approaches, the protein inhibiting miR-675 processing at least in part was identified as the RNA-binding protein HuR. HuR binds the full-length H19 RNA and inhibits the processing of miR-675, probably at the Drosha step. Furthermore and using an H19 mouse model carrying a 3-kb deletion of just the H19 transcription unit, including miR-675 to exclude the effect of IGF2, it was shown that placental overgrowth results, implying that miR-675 is a negative regulator of placental size. Apart from regulating the abundance of IGF2 through imprinting, the H19 locus can also regulate IGF2 abundance through targeting its receptor, IGF1R, by miR-675. Increased levels of miR-675 in the placenta coincide with downregulation of IGF1R that may contribute, at least in part, to the growth inhibiting effect on the placental size [11].

miR-675 has been assigned a contradictory role in the process of proliferation, and it seems to function differently in normal versus cancer cells. Under normal conditions, miR-675 inhibits human trophoblast cell proliferation by directly downregulating Nodal Modulator 1 (NOMO1) protein expression, binding to the 3′-UTR sequence of NOMO-1. NOMO1 is an antagonist of Nodal, which could attenuate Nodal signaling [12]. Moreover, it was shown that miR-675 slows cell proliferation and, thus, can limit placental overgrowth, as discussed above. However, both H19 and miR-675 were found to be upregulated in human colon cancer, both in cell lines and primary colorectal cancer biopsies relative to adjacent non-cancerous tissues. Moreover, an inverse correlation was observed between the expression of retinoblastoma (RB) and H19/miR-675. Through both over-expression and knockdown approaches, the oncogenic property of miR-675 was revealed. Suppression of miR-675 decreased cell growth and soft agar colony formation in human colon cancer cells, while overexpression increased cell growth and soft agar colony formation. This phenotypic effect of miR-675 could be performed at least in part by targeting the tumor suppressor, RB [13].

A lot remains to be performed, mainly in the identification of the miR-675 targets and understanding its regulation and function. In adult human chondrocytes, expression of H19 (and subsequently miR-675) is driven by SOX9 to positively regulate COL2A1, which encodes a collagen protein important to the cartilage matrix [14].

We have reported the identification of an alternative splice isoform of H19 RNA that lacks part of exon 1. This variant was detected in human embryonic and placental tissues, but not in bladder or hepatocellular carcinomas. A very low level of this variant was also detected in colon carcinoma. The observed pattern of expression suggests that this splice variant is developmentally regulated and that it plays a role in normal embryonic development, rather than in oncogenesis [5].

In principle, a minor transcript, such as the one described here, could function in several different ways to produce a biological phenotype. The change in the secondary structure resulting from splicing, as deduced from computational analysis, could indicate a special role for this variant in a certain developmental window. Another possibility is that its activity resides in the sequences at the splice points embedded within the primary transcript, rather than in the mature mRNA itself [5].

Another possibility is that this alternative spliced variant affects HOTS protein or miR-675 processing.

An additional alternative splice variant of H19 has been reported. This variant transcript, which lacks exon 4, is either not found at all, is widely expressed or is confined to extra-villous cytotrophoblasts in first trimester placenta, depending on a combination of the genotype and the sex of the transmitting parent. This variant is genotype-specific [6].

Every solid tumor encounters hypoxic regions when grown beyond certain diameters. Hypoxia is considered a major trigger for a number of pathways that have substantial impacts on tumor progression affecting tumor angiogenesis, metastasis and chemo-resistance. It is also associated with poor prognosis, at least in some types of human cancers. All of these conditions are associated with H19 RNA upregulation [15–18]. As hypoxia readily occurs in the majority of solid tumors, driving critical steps in tumor development and metastasis, it is of great interest to identify signaling pathways involved in this fatal outcome. In our recent studies, we identified hypoxia as a key trigger that activates the expression of the H19 gene, and we also uncovered a major transcriptional interplay between both positive and negative regulators dictating H19 expression under hypoxic stress. Furthermore, H19 downstream targets have been identified using both overexpression and knockdown approaches [17,18].

Following our initial study showing H19 induction upon hypoxia in certain cell lines, we screened about thirty different carcinoma cell lines of different lineages and origins for their ability to induce H19 RNA in hypoxic stress [18]. Cells respond differently to hypoxic stress in terms of H19 modulation. To gain insight into the possible mechanism associated with the H19 response to hypoxia, we searched for a common denominator among those cell lines that do not upregulate H19 upon hypoxia.

HIF-1 and p53 are two of the most intensively studied transcription factors; both factors are involved with hypoxic stress adaptation and are responsible, at least in part, for the above listed phenotypes of the tumor triggered by hypoxic stress. Both factors are maintained at low or undetectable levels within non-stressed cells, but are rapidly stabilized as a result of post-translational modifications, hydroxylation of HIF-1 and phosphorylation of p53. HIF-1 signaling is critical for mediating cellular adaptation to hypoxia, whereas p53 promotes hypoxia-induced apoptosis. The outcome of this interplay has major consequences on tumor progression.

We recently demonstrated a tight correlation between H19 RNA elevation by hypoxia and the status of p53. Cells harboring wild-type p53 (p53^wt) do not induce H19 RNA in their response to hypoxia, whereas in cells carrying a mutated p53 (p53^mt), the H19 message is significantly induced, most strongly in p53-null cells.

Additionally, through various approaches, we identified HIF1-α as the factor responsible for H19 elevation under hypoxic stress [18].

In light of our study, a molecular mechanism integrating H19, p53 and HIF1-α to hypoxic stress response is uncovered. In p53^wt cells, simultaneous suppression of p53 and overexpression of HIF1-α are needed to induce H19 significantly, while each treatment separately results in a mild induction, indicating that the molecular mechanism of p53 suppression on H19 may, at least in part, involve interfering with HIF1-α activity [18].

Our findings suggest that H19 induction upon hypoxia results from loss of p53 function and HIF1-α increased activity observed in a large variety of human cancers (Figure 2). Our earlier observation that H19 modulates genes whose expression is functionally involved in angiogenesis, survival and tumorigenesis in hypoxic stress indicates that H19 RNA could grant a selective advantage to tumor growth under stress conditions [2,12], which are important phenotypes resulting from p53 loss of function and HIF1-α increased transcriptional activity (Figure 2).

In accordance with this, several lines of evidence support the involvement of H19 RNA in tumor progression through the metastatic pathway triggered by hypoxic stress. H19 RNA alters expression profiles of genes involved in metastasis and blood vessel development, supporting the notion of a role for this gene in tumor invasion and angiogenesis. Moreover, H19 is highly expressed in a large proportion of hepatic metastases tested. The level of H19 expression was also strongly correlated with tumor invasion of the reproductive organs and significantly correlated with neoplastic cell invasion of the myometrium. Moreover, the H19 gene is expressed within both epithelial and stromal components of human invasive adenocarcinomas, where high expression matches tumor invasion.

When epithelial cells acquire mesenchymal, fibroblast-like properties and show reduced intercellular adhesion and increased motility, this process is termed epithelial-to-mesenchymal-transition (EMT). EMT is critical for embryonic development in multicellular organisms. Moreover, EMT is a potential mechanism for carcinoma progression. Our preliminary results linked H19 upregulation to the process of EMT in carcinogenesis and embryogenesis. Induction of EMT in cancer cells by different approaches (e.g., hypoxia, TGFβ) is accompanied by H19 upregulation.

c-Myc is one of the transforming members of the Myc family and functions as a transcription factor. It obligatorily heterodimerizes its partner, Max, to bind DNA sequence elements, called E-boxes, and uses various mechanisms to allow target gene transcription. Numerous gene targets have been identified for c-Myc, including those functioning in proliferation, apoptosis, transformation and angiogenesis, however, little is known regarding the transcriptional target(s) of c-Myc responsible for its strong transforming abilities.

One of the transcriptional targets of c-Myc is H19 non-coding RNA. A strong association between H19 and c-Myc expressions was evident in both primary breast and lung cancer biopsies. c-Myc strongly induces the expression of H19 and binds directly to unmethylated E-boxes close to the imprinting control region. c-Myc specifically binds and regulates the active maternal allele, but not the silenced paternal allele. It was shown that the histone acetylation activity is recruited by c-Myc to the H19 promoter, leading to its activation without affecting the imprinting of the H19/IGF2 locus [19].

Given the strong association of H19 and Myc expression, the essential role of H19 in transformation suggests that Myc-induced H19 expression contributes to tumor etiology and the strong oncogenic behavior of Myc[19].

E2F transcriptional regulators control human-cell proliferation by repressing and activating the transcription of genes required for cell-cycle progression, particularly the S-phase. Their associations and binding to E2F-responsive promoters are cell-cycle selective. The first member of this protein family to be cloned is the E2F1 and is largely considered to be the critical factor for G1/S-phase transition through the regulation of the transcription of several gene products needed for DNA synthesis. Furthermore, E2F1 is involved in tumorigenesis of several types of human cancers.

Our previous works have shown that overexpression of the H19 gene can override cell growth arrest and induce cells to enter the S-phase in serum starved conditions accompanied by suppression of the expression of p57Kip2[20]. This is consistent with the results obtained from other group showing that H19 RNA is important for entry into the S-phase after recovery from serum starvation by E2F binding to its promoter [21]. Moreover, H19 is suppressed by the tumor suppressor p53 [22]. As discussed above, miR-675 targets the tumor suppressor, RB. All of these observations place H19 in the core of cell cycle control especially in the transition from G1- to S-phase.

A correlation between H19 and E2F1 expression levels in breast cancer was also revealed. Both genes are weakly expressed in normal breast cells, but upregulated in breast cancer [21].

However and through overexpression and knockdown approaches, we cannot detect a significant effect for H19 on cell proliferation under normal cell growth conditions [20]. Under stress conditions of serum starvation and hypoxia, H19 confers a clear growth advantage. Hypoxia and serum starvation are both the consequences of a poorly vascularized tumor, which is considered a normal stage during tumor development. Our results indicate the importance of H19 gene expression for the tumor under stress conditions, induced by poor vascularization and characterized by poor oxygen and growth factors availability.

We previously hypothesized on the possible role played by H19 RNA in tumorigenicity. The microenvironment of the tumor is the factor that imposes the selective pressure on the malignant cells. H19 expression, occurring in a malignant cell and possibly enhancing its ability to proliferate under harsh condition, will give that cell a selective advantage. The progeny of the H19-expressing cells will increase in number at a higher rate than the neighboring cells and, hence, gradually increase their relative contribution to the tumor volume [15].

Phenotypic traits beneficial for cell proliferation also seem to favor invasive growth and metastasis. In stressed condition, those cells that manage to proliferate will indeed contribute greatly to the generation of a patho-physiological microenvironment with low extracellular pH (more acidic) and low oxygen tensions (hypoxia). Experimental studies have shown that hypoxic tumors may also be pro-angiogenic and pro-metastatic. Hypoxic conditions in tumors induce the release of cytokines that promote vascularization and, thereby, enhance tumor growth and metastasis.

Since we provide evidence that H19 RNA enables the cells to continue proliferating in a serum starved and hypoxic condition (one of the consequences of a poorly vascularized tumor), it is logical to assume that the relative contribution of H19 expressing cells towards the creation of the pathological microenvironment is great, which will promote tumor angiogenesis, invasion and metastasis.

Beckwith–Wiedemann syndrome (BWS), a somatic overgrowth disorder with predisposition to embryonic tumors, is known to be caused by various epigenetic and genetic alterations, which affect regulation of the imprinted genes located on chromosome 11p15.5[23]. The imprinting center 1 (ICR) that resides between the IGF2 and H19 loci is normally differentially methylated, leading to IGF2 expression from the paternal chromosome together with silencing of H19 expression. However, in 2%–7% of BWS patients, both alleles are methylated, leading to IGF2 loss of imprinting and loss of H19 expression (H19 epimutation). This gain of methylation leads also to predisposition to develop Wilm’s tumor, hepatoblastoma and other childhood tumors [23]. However, IGF2, rather than H19, is the key factor in the development of BWS, since in many cases of BWS, normal methylation and expression of H19 is accompanied by IGF2 bi-allelic expression [24].

Russell—Silver syndrome (RSS) is a heterogeneous disorder associated with growth restriction (both pre- and post-natally) and relative macrocephaly. As opposed to its reported hypermethylated status in BWS, ICR1 on chromosome 11p15.5 is significantly hypomethylated in ~20%–60% of RSS patients [25]. Regarding the complementary phenotypes of RSS and BWS, lack of IGF2 due to epimutation, rather than H19 bi-allelic expression, forms the basis of this syndrome, although a transgenic mouse model overexpressing H19 seems to suggest that H19 transcription levels have a trans-effect on gene imprinting in the embryo and on IGF2 levels [26]. However, one study does suggest a functional role for H19 transcripts in RSS etiology [27]. In this study, a cohort of 44 SRS patients was screened for variations in the transcribed region of H19. In two of the patients, different single 3 bp deletions, confined to exon1, were identified. In a third patient, 39 bp duplication was identified across exon 2 and intron 2. In two of the three patients, an abnormal H19 splicing pattern was detected by in vitro studies. However, lymphocytes analysis of one of these two patients carrying the duplication did not verify an altered expression pattern of H19. Thus, it is possible that H19 transcripts have a role in SRS etiology—either as an epigenetic factor or as an active noncoding RNA with altered functions.

The connection of the H19 locus to growth disorders may suggest a possible involvement of the H19 locus in being overweight and obesity. Indeed, it was reported that one-year-old children who were overweight or obese had significantly higher methylation percentages at the H19 DMR at birth compared with children who were not overweight or obese [28]. Moreover, it seems that, as a response to starvation during periconception, ICR1 becomes hypermethylated, leading to restricted growth due to lower IGF2 expression in adult life. Individuals who experienced famine prenatally during the second world war had hypomethylated IGF2 DMR 60 years later, compared with their same-sex siblings that did not experience hunger [29]. H19 DMR was not significantly associated with exposure to hunger in those individuals; however, the implications of the methylation profile reported on H19 expression levels in the cohort above were not detected. Apparently, also here, IGF2 is the key factor in the process.

Since inflammation, especially chronic, can cause cancer [30] and since H19 is a major player in many cancer types, the question arises whether H19 regulation/expression may change during the inflammatory process. One model that was thoroughly examined for H19 expression in this context is rheumatoid arthritis (RA) [31], an inflammatory disease resembling cancer in many features, like, for example, the metastatic-like invasiveness of the synovial tissue into cartilage and bone, expression of several proto-oncogenes and mutations in p53. As mentioned above, H19 is upregulated in hypoxic cancerous cells, as well as upon starvation stress and reacts to several stress related factors, such as thioredoxin, MMK1, NF-Kb, JNK2, TNF-α and IL-6. The synovial tissue in RA is also under oxidative stress. Comparing RA synovial tissue to osteoarthritis and normal/joint trauma controls revealed a higher expression of H19 transcripts both in situ and by semi-quantitative PCR. RA synovial tissue-derived cultured fibroblasts elevate their H19 level following starvation, as compared to the control cultures mentioned above, in which starvation needed an additional stimulation, such as IL-1β or PDGF-BB. However, since the change observed was mainly quantitative rather than qualitative, H19 cannot be regarded as a tumor marker in RA, since it is also expressed in chronic inflammatory diseases, such as osteoarthritis and normal/joint trauma However, H19 may support dedifferentiation of the RA synovial tissue and a risk for tumor development. The correlation between this risk, which indeed exists for several cancers [32,33] and H19 levels in the RA synovial tissue is yet to be tested. It is worth noting, however, that in a study looking at 100 patients, several tumor markers were found to be elevated in RA patients’ serum without any predictive value for tumor development [34]. Hence, H19 elevation in RA may reflect only the inflammatory stress, without further interpretations.

Pre-eclampsia (PE) is a gestational hypertension, which affects 2%–7% of pregnancies (threatening both, mother and fetus lives) worldwide and is considered as the most common dangerous complication of pregnancy. Its symptoms disappear following the removal of the placenta and, hence, is regarded as a placental disease [35]. Since imprinting is a placenta-related process and H19 null mice display hyperplasia of all layers of the placenta [36], H19 involvement in its pathology is not surprising. Screening of women’s placentas has revealed H19 LOI in 46.15% of pre-eclamptic patients (disregarding the chronologic onset of the disease), but no LOI in the healthy control group. Moreover, in the pre-eclamptic group, severe clinical symptoms (blood pressure and urine protein) were observed in the biallelic expressing group, compared to patients with monoallelic expression [37]. However, the status of H19 imprinting in these patients was not correlated with H19 transcription levels, which did not increase in the biallelic expressing group. This observation may be explained by post-transcriptional, alternative regulation levels of H19 transcript levels, which obviate the regulation by imprinting. Additionally, miR-675 levels were not examined in this study, although they may differ between the groups in the study. It is worth noting that in a French study, in which villous cytotrophoblasts were isolated from PE patients and compared to control cells from healthy patients grown under normoxic or hypoxic conditions, it was found that many of the hypoxia induced genes were also induced in PE (which may reflect the hypoxic stress during improper placentation in PE). Among the genes induced in both healthy hypoxic cells and PE cells was H19, which, as mentioned above, is known to be induced by hypoxia [38].

Nevertheless, the nature of the relevance of H19 to PE is still controversial. In a Canadian study of PE patients that screened for methylation levels in H19/IGF2 ICR1, no differences between healthy control placentas and PE placentas were observed [39]. However, other studies, also in the Chinese population [40], showed that global methylation, together with DNA methyltransferase 1 transcription levels, were increased in placentas with early onset of PE. H19 promoter methylation levels were also increased within these placentas, and this methylation status was also expressed in reduced transcription levels of H19. Since H19 is mostly expressed in the invasive intermediate trophoblasts [41] and villous cytotrophoblasts, but abundant in syncytiotrophoblasts [42,43], it may be regarded as an invasion-promoting factor in trophoblasts, possibly supporting proper placentation. Further to this study, in vitro assays in trophoblasts cultures revealed that H19 has anti-proliferation effects in culture, mediated by miR-675[12]. Deeper analysis showed that miR-675 levels decrease in patients with early PE onset, and this decrease was suggested to mediate an increase in NOMO1 protein levels, a suppressor of the anti-proliferative and pro-apoptotic Nodal pathway [12].

In conclusion, observations concerning H19 expression and function in PE etiology should be standardized before it may (or may not) support usage of H19 as a biomarker for estimating the risk of developing PE [44].

In superficial transitional cell carcinoma of the bladder, a Phase 1/2a dose escalation, safety and preliminary efficacy study was completed and a Phase 2b clinical trial has completed accrual under a US Investigational New Drug (IND) application.

The phase 1 study enrolled patients with recurrent superficial TCC of the bladder, which had relapsed after prior BCG therapy and expressed H19 RNA. A total of 18 patients were treated with intravesical BC-819 at doses of 2–20 mg weekly and could receive periodic maintenance therapy for up to one year. This was a heavily pre-treated patient population.

Median time to recurrence among all 18 patients was 5.7 months (95% CI 4.1–11.6). One-year recurrence-free survival was approximately 30%. Treatment was well-tolerated. No severe toxicity was observed and no deaths occurred during the study or follow-up period. The most frequently reported adverse events (AEs) considered at least possibly related to investigational product for any dose cohort were mild to moderate in severity and were most commonly renal and urinary disorders. Therefore, the dose of 20 mg was selected for the Phase 2b study [45].

A Phase 2b study multicenter trial of intravesical BC-819/PEI in patients with intermediate-risk superficial bladder cancer is being completed in patients with histologically confirmed recurrent superficial bladder cancer who failed prior therapy with BCG and chemotherapy. Patients with carcinoma in situ were excluded. Patients received an induction phase of six weekly treatments, followed by a safety and efficacy assessment at week 9. Subsequently, in the absence of recurrence or toxicity necessitating discontinuation of therapy, patients received three three-week courses of BC-819/PEI maintenance therapy every 12 weeks for up to one year.

A total of 47 patients were recruited, 39 formed the per-protocol population, eight treated patients were not evaluable due to various protocol violations and were replaced. Among the first cohort, 9/18 patients (50%) had complete resolution of the target lesion at visit 7 (week 8–10). For all patients entered, three-months and one-year recurrence-free survivals are 63% and 48%, respectively.

Treatment has been well-tolerated. No patients have discontinued due to treatment-related AEs. The most commonly reported AEs were urinary tract disorders, such as urinary frequency and dysuria, in 34% of patients treated, all of which were mild or moderate. No treatment-related serious adverse events have been reported, except one case of possibly related hematuria.

A Phase 1/2a dose escalation safety and preliminary efficacy for the treatment of patients with locally advanced unresectable pancreatic cancer was completed.

In a phase 1 study, nine patients with unresectable locally advanced pancreatic carcinoma (LAPC) received four doses each of intratumoral BC-819 at either 4 or 8 mg per dose. Treatment was well-tolerated with no treatment-related AEs, and the maximum tolerated dose (MTD) was not reached. Three patients in the 8 mg cohort demonstrated partial response (PR) at their three-month assessment [46].

A phase 2b study testing higher doses of BC-819 in combination with gemcitabine, the standard drug used, is currently ongoing in Israel and in the US to assess efficacy and safety in locally advanced, unresectable pancreatic adenocarcinoma. Patients received gemcitabine weekly for four weeks and were then randomized to 8 or 12 mg of intratumoral BC-819 administered via endoscopic ultrasound for a core treatment of seven administrations of BC-819 together with six additional infusions of gemcitabine. Patients could continue on periodic maintenance with BC-819 and gemcitabine, as long as they did not progress. Twelve patients have completed the first part of the study; 11/12 patients were evaluable for response. At their three-month assessment, 9/11 patients showed partial response (n = 2) or stable disease (n = 7). The adverse event profile in these patients was in line with that expected in a patient population with locally advanced pancreatic adenocarcinoma. All patients experienced AEs, mostly gastrointestinal or general disorders or laboratory abnormalities, primarily in liver function. No serious adverse event was considered by an investigator to be related to BC-819.

A Phase 1/2a dose escalation safety and preliminary efficacy study for the treatment of patients with advanced stage ovarian cancer has been completed. In addition, a patient with ovarian cancer was treated under a compassionate use protocol received sixteen IP infusions of BC-819 at doses ranging from 80 mg to 140 mg of plasmid DNA per treatment for a total cumulative dose of 1.7 g; this was well-tolerated [47].

In the Phase 1/2a study, 14 subjects with recurrent, platinum resistant advanced stage ovarian cancer or primary peritoneal carcinoma were treated with intraperitoneally administered BC-819. These heavily pre-treated patients received escalating doses of 60–240 mg of BC-819. Again, the MTD was not reached. The majority of the AEs were laboratory abnormalities, general or gastrointestinal disorders mostly related to the patients’ general medical condition rather than to BC-819. The highest cumulative exposure by IP administration in this study was 720 mg to three subjects in the highest dose cohort (three administrations each of 240 mg). This dose was well-tolerated in all cases.

The best tumor response was stable disease; no patient demonstrated a complete or partial remission. As most patients had ascites, which often required paracentesis, standard assessment of response was problematic. A dose response effect on survival was observed, indicating an antitumor effect, though this should be interpreted with caution in the light of the small sample sizes and possible confounding variables among cohorts.

It was shown in animal tumor models that the administration of BC-819 is safe and efficacious in the hepatic cancer indication and preliminary evidence of tumor response was obtained in two compassionate use patients with hepatic metastases.

Two patients with colon liver metastases were treated during a named patient compassionate use program (one by intratumoral route of administration and one by hepatic artery infusion). The intratumoral injections were two doses of 6 mg each. The treatment was well tolerated, provided temporary palliative relief and showed radiographic evidence of a large area of tumor shrinkage. The second case was a patient with inoperable metastasis in both lobes of the liver. The patient received two courses of treatment each consisting of three infusions of BC-819 via the common hepatic artery given once per week for three weeks, with the second course starting one month after the first infusion. The first course consisted of escalating doses of 16, 24 and 36 mg of BC-819 DNA. The second course consisted of escalating doses of 48, 64 and 82 mg of BC-819. This patient had stable disease throughout the two months of treatment.