Background
Colorectal cancer (CRC) is the third most common type of cancer, constituting approximately 9.4% of all cancers diagnosed, and the third leading cause of cancer death. Approximately, 25% of patients diagnosed of colorectal cancer have already metastatic spread, and 25% of initially localized disease will develop metastases [
1]. The recommended strategy for locally advanced colon cancer consists of preoperative combined chemo and radiotherapy, followed by surgery and then by adjuvant chemotherapy, to reduce both the local recurrence and the possibility of distant relapse [
2]. Adjuvant chemotherapy in stage III colon cancer is fully justified. The combination of 5-fluorouracil (5-FU) and folinic acid (leucovorin), which enhances 5-FU effects by inhibiting thymilydate synthase, administered for six months, or oral fluoropyrimidines such as the 5-FU prodrugs capecitabine [
3] or tegafur [
4], are able to reduce the risk of death by 30%, assuming an absolute increase of 10-13% in terms of survival. Further combination of oxaliplatin either to the regimen of 5-FU and folinic acid or to capecitabine increased survival in this group of patients [
5-
7]. Indication and treatment of stage II disease is controversial and depends on clinical and histological risk factors [
8]. Considering advanced disease, first-line chemotherapy including the combination of folinic acid with continuous infusion of 5-FU, along with oxaliplatin (FOLFOX) or irinotecan (FOLFIRI) are reasonable choices, with comparable effectiveness in terms of objective responses and survival [
9]. Capecitabine combinations have shown similar efficacy to continuous infusion of 5-FU combinations [
10-
13]. Bevacizumab, a humanized monoclonal antibody against vascular endothelial growth factor (VEGF), and cetuximab, a monoclonal antibody directed against the extracellular domain of the epidermal growth factor receptor (EGFR), have demonstrated an additive effect on chemotherapy, therefore broadening the options for treatments of patients in first and consecutive lines [
14,
15]. However, anti-EGFR therapy is only recommended in KRAS/BRAF wild type patients.
Recently, we have established primary cultures obtained from patients with CRC cancer. The novel colon cancer cell line HGUE-C-1 was obtained from ascitic efussion of a 76-year old man with colon cancer. The patient was initially admitted at the hospital, in November 2003. A complete colonoscopy was performed, showing a mass eight centimetres long, starting eighteen centimetres far from the anal verge. The biopsy confirmed diagnosis of colon adenocarcinoma. R0 down anterior resection was performed, resulting in a moderately differentiated colon adenocarcinoma affecting serosa, with two out of eleven metastatic lymph nodes (GII pT3 N1b). After postoperative evaluation consisting of thorax-abdomen-pelvic CT scan which showed no evidence of residual disease, and carcinoembrionary antigen (CEA) value in the normal range, adjuvant chemotherapy with 5-FU and folinic acid was administered for six months. After completing adjuvant chemotherapy, there was no suspect or evidence of relapse by imaging tests and blood analysis. The patient entered at that time onto a scheduled follow-up programme. Two years later, the patient was admitted into the hospital due to an increase in the abdominal perimeter. Thorax-abdomen-pelvic CT scan revealed massive ascites. The cytology performed on ascitic fluid obtained after diagnostic paracentesis confirmed colon adenocarcinoma origin of the ascites. Palliative chemotherapy was then started with capecitabine and irinotecan. After a second cycle of chemotherapy, the patient was admitted into the hospital due to grade III chemotherapy-induced diarrhea. During admission, two parecenteses of malignant haematic ascites with 72 hours interval were performed (5,000 and 5,400 ml). The patient received a third cycle of treatment on an outpatient basis with 25% reduction in doses of capecitabine and irinotecan. Seven days after beginning of the third cycle, the patient was again admitted into the hospital due to grade III diarrhea associated to renal failure. The patient showed no response to medical procedures, and considering the global prognosis, exclusive symptomatic treatment was decided. Patient died eight days after final admission.
The new HGUE-C-1 cell line constitutes an interesting model of study from several points of view. Initially, we determined whether HGUE-C-1 cells presented the microsatellite instability (MSI) phenotype, already known to be related to colorectal carcinogenesis in about 15% of all CRC [
16]. Interestingly, HGUE-C-1 cells did not show MSI phenotype. HGUE-C-1 cells were also analysed for mutations in
KRAS,
BRAF,
PIK3CA and
TP53 genes, which are quite commonly mutated in colon carcinoma and have been related to colon carcinogenesis [
17-
19]. Further analysis with the dinucleotide polymorphic repeat marker D5S346 showed loss of heterozygosity affecting the Adenomatous Polyposis Coli (APC) containing region in chromosome five and nuclear staining of β-catenin protein, suggesting that the APC signalling pathway was modified in HGUE-C-1 cells.
HGUE-C-1 cells are also interesting as an experimental model for the study of chemoresistance in patients with colon cancer. In this sense, HGUE-C-1 cells show resistance to 5-FU and irinotecan. This cell line constitutes a better physiological model for chemoresistance studies in comparison with other cell lines that become resistant in vitro by selective pressure after treatment with increasing concentrations of specific drugs.
HGUE-C-1 represents an established cell line derived from primary cultures of a biological sample obtained from a patient, in the context of a general project aimed to the development of predictive tests with a panel of different alternative treatments. In this context, a complete pharmacological profile of HGUE-C-1 cells was performed. Interestingly, the HGUE-C-1 cell line showed chemosensitivity to EGFR inhibitors erlotinib, gefitinib, the dual PI3K/mTOR inhibitor NVP-BEZ235, the mTOR inhibitor rapamycin, the histone deacetylase inhibitor trichostatin (TSA) among other drugs, being partially resistant to the heat shock protein 90 (Hsp90) inhibitor 17-allylamino-17-demethoxygeldanamycin (17-AAG), and totally resistant to the Mek inhibitor AZD-6244 (Selumetinib) and to the chemotherapeutic agent oxaliplatin, despite that the patient was not treated with such drugs. The putative molecular mechanisms involved in HGUE-C-1 carcinogenesis, and drug chemosensitivity or chemoresistance will be discussed herein.
Methods
Cell culture
The human colorectal cancer cell lines HT-29, SW620, SW480, HCT-15 and HCT-116 cells were obtained from the Instituto Municipal de Investigaciones Médicas de Barcelona (Spain), HT-29, SW480, HCT-15, HGUE-C-1, SW620 and HCT-116 cells were maintained in Dulbecco’s modified Eagle’s medium (DMEM) (Labclinics SA, Barcelona, Spain) supplemented with 10% heat-inactivated fetal bovine serum (FBS) (Labclinics), 50 U/mL of penicillin and 50 mg/mL streptomycin (Labclinics) and incubated at 37°C in a humidified 5% CO2/air atmosphere.
Reagents
Gefitinib, erlotinib, sorafenib, 17-AAG, NVP-BEZ235 and AZD-6244 were obtained from ChemieTek (Indianapolis, IN, USA). Rapamycin, tricostatin (TSA), propidium iodide and 3-(4, 5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) were purchased from Sigma-Aldrich (St. Louis, MO, USA). RNase A was obtained from Serva (Heidelberg, Germany).
Cell proliferation assays
Cell proliferation was assessed using the MTT assay based on the activity of the mitochondrial enzyme succinate dehydrogenase. Colorectal carcinoma cells were seeded in 96-well plates at a density of 2,500 cells per well and incubated at 37°C with 5% CO2. Increasing doses of the indicated drugs were added, with DMSO as non-treated control. The dose range for each drug was selected taking in consideration the maximal and the minimal concentration of the drug in patient´s plasma and/or previous MTT assays dose response studies in our panel of colon cancer cell lines. The culture was continued for 72 hours and at the end of the treatment, 30 μl of MTT solution (5 mg/ml in PBS) were added into each well, followed by incubation at 37°C for three hours. The culture medium containing MTT was aspirated and the formazan crystals formed were then solubilized with 200 μl DMSO for 30 minutes. Absorbance was measured at wavelength 570 nm in a microplate reader (Anthos 2001 Labtec Instruments GmbH, Wals, Austria), and the percentage of proliferation of HGUE-C-1 and HT-29 cells was determined for each concentration of the indicated drug. Both treatment and control groups were performed in 6 replicate wells and the experiment was repeated at least three times to ensure the data reproducibility.
Cell cycle analysis
Cells were cultured in T25 flasks and treated with the different drugs at the indicated concentration with DMSO as non-treated control. At the end of the treatment, both floating and adherent cells were collected, combined, washed with PBS, and fixed with 500 μl of chilled 70% ethanol in PBS at −20°C. Following fixation, cells were pelleted and resuspended in 500 μl of PBS containing 0.5% Triton X-100, 25 μg/ml RNase A and 25 × 10−3 μg/ml propidium iodide. After 30 minutes at room temperature in the dark, cell cycle distribution was determined with an Epics XL flow cytometer (Beckman Coulter Co., Miami, FL). When the fluorescence is less than the fluorescence peak corresponding to that of the G0/G1-phase, cells are considered to be apoptotic (sub-G1).
Western blot analysis
Cells were plated for different times in serum-starved conditions, lysed in NP-40 lysis buffer (50 mM Tris–HCl pH 7.4, 1% NP-40, 150 mM NaCl, 5 mM EDTA, 50 mM NaF, 30 mM Na4P2O7, 1 mM Na3VO4,) with a protease inhibitor cocktail (Sigma-Aldrich) for 30 min on ice. After centrifugation at 15,000 x g for 5 minutes at 4°C, the supernatants were collected and the protein concentration of the cell lysates was determined by the Bradford method (Bio-Rad, Richmond, CA). Total protein content (60–80 μg) from each lysate was electrophoresed on 10% polyacrylamide gels in the presence of sodiumdodecyl sulfate (SDS) and transferred onto nitrocellulose membranes. Nonspecific sites were blocked incubating for 1 hour at room temperature with 5% non-fat dry milk. Membranes were then incubated overnight with the indicated primary antibodies. EGFR and HER3 antibodies were purchased from Santa Cruz Biotechnology (Santa Cruz, CA, USA); phospho-ERK1/2, ERK1/2, phospho-p70S6K, p70S6K, phospho-RPS6 and RPS6 antibodies were purchased from Cell Signaling Technologies (Danvers, MA); Retinoblastoma antibody was purchased from BD Biosciences (San Jose, CA); actin antibody was purchased from Sigma-Aldrich. The primary antibodies were incubated with secondary antibodies linked to horseradish peroxidase (GE Healthcare, Buckinghamshire, UK). Specific proteins were visualized by enhanced chemiluminescence detection using the ECL system (GE Healthcare), according to the manufacturer’s instructions.
Transfection and luciferase measurement
HT-29 and HGUE-C-1 cells were seeded in 24-well culture plates (180,000 and 150,000 cells/well, respectively). When cells reached 40–60% confluence (24 hr), they were transiently transfected with 0.8 μg of pRb-TA-Luc or pE2F-TA-Luc responsive luciferase reporter plasmid (Clontech, Mountain View, CA), using Lipofectamine2000 reagent (Invitrogen, Carlsbad, CA, USA) in a DNA transfection agent ratio of 1:3. The pTa-Luc vector lacking the response element was used as negative control. Six hours after transfection, culture medium was replaced by fresh medium and cells were kept under normal growth condition in DMEM with 10% foetal serum for 24 hours prior to lysis and luciferase detection. All transfections were performed as co-transfections using a Renilla luciferase expression plasmid (Promega Corporation, Madison, WI) to establish an internal control for transfection efficiency. The transfected cells were washed once with PBS and lysed using 100 μl Passive Lysis Buffer (Promega). Firefly and Renilla luciferase activities were determined using the Dual-Luciferase Reporter Assay System (Promega) according to the manufacturer’s instructions, using for detection of the chemiluminescent signal, a luminometer from Berthold (Montreal Biotech, Kirkland, QC). Promoter activities of the RB and E2F reporter plasmids were expressed using the arbitrary units “RLU” (relative luciferase units).
HGUE-C-1 genetic analysis
DNA from different passages of HGUE-C-1 cells was isolated using the DNeasy Blood & Tissue Kit (Qiagen, Valencia, CA). HGUE-C-1 cells were screened for MSI status by multiplex PCR using the pentaplex set of monomorphic markers (BAT 26, BAT 25, NR21, NR24 and NR27). Mutations in BRAF (V600E) and KRAS (codon 12/13) were identified by direct sequencing. Primer sequences were BRAF:F-TGCTTGCTCTGATAGGAAAATGA, BRAF:R-TGGATCCAGACAACTGTTCAAA, KRAS.F-GCCTGCTGAAAATGACTGAA and KRAS:R- AGAATGGTCCTGCACCAGTAA. PCR products were purified using a QIAquick PCR purification kit (Qiagen) and directly sequenced on an ABI PRISM 3100 sequencer (Applied Biosystems, Foster City, CA). Presence of PIK3CA mutations in exons 9 and 20 were determined by direct sequencing after a nested PCR reaction. Amplicons were purified and subjected to direct sequencing using exosap-kit (USB Corporation) and sequenced using the primers PI542-5IF and PI542-5IR for exon 9 and PI1047IF and PI1047IR for exon 20 with BigDye Terminator Sequencing Kit and ABI PRISM 3100 sequencer (Applied Biosystems). TP53 gene mutations were determined on genomic DNA from two different culture passages, p3 and p30, of HGUE-C-1 cells. Mutations in exons 4–11 were analysed by PCR amplification and direct sequencing of the coding sequence and exon-intron boundaries. The PCR amplified products were purified and sequenced. Three dinucleotide polymorphic repeat markers (D2S123, D5S346 and D17S250) were amplified by PCR using fluorescent labelled primers and analysed by capillary electrophoresis in an ABI PRISM 3100 sequencer (Applied Biosystems). The size of the markers was compared at two different cell culture passages p3 and p45.
Immunohistochemistry
Three-micrometre sections were cut from paraffin-embeded tumour specimens and the slides were pretreated in a PT link from Dako (Glostrup, Denmark) and incubated with antibodies against β-catenin. Signal amplification and development were carried out with EnVision Flex kit (Dako), according to the manufacturer’s instructions.
Ethics statement
Ascitic efussion (from where HGUE-C-1 cells were derived) of a patient with colon cancer was obtained according to institutional guidelines with the approval of the “Comité Etico y de Investigación Clínica” (Clinical Research and Ethics Committee) Review Board, Hospital General Universitario de Elche, Elche, Spain. This ethics committee waived the need for informed consent for this particular kind of human samples.
Discussion
Herein we have characterized a new colon carcinoma cell line, HGUE-C-1, obtained from the ascitic fluid from a 76 years old patient with colon cancer. HGUE-C-1 cells represent an interesting model of study from different points of view. First, this cell line has been obtained from a tumour that belongs to a group of colon carcinomas lacking MSI, with loss of heterozygosity affecting the APC locus, and without
TP53,
KRAS,
BRAF or
PIK3CA mutations. These molecular characteristics are representative of less than 12% of all colon carcinomas [
20]. Second, an extensive pharmacological profile of this cell line indicates that it represents a physiological model of chemoresistance (developed inside the patient) to 5-FU and irinotecan, drugs that have been used to treat this patient. Third, HGUE-C-1 cells show partial or total cross-resistance to drugs never used in the patient before, such as cetuximab, 17-AAG, oxaliplatin or AZD-6244. Finally, HGUE-C-1 cells are still sensitive to other drugs such as TSA, rapamycin, BEZ-235, sorafenib, erlotinib, gefitinib and others, suggesting that different pathways can still be targeted in patients with similar pharmacological profile and genetic background than the patient from which HGUE-C-1 cells were obtained.
As mentioned above, HGUE-C-1 cells are quite atypical when compared with other colon carcinoma cell lines, or when we analyse the usual genetic changes reported in colon carcinoma patients. In this sense, it is known that around 10-15% of colon carcinomas have MSI phenotype [
21] and 50-55% of tumours carry mutations in
TP53 [
22]. Similar percentages of mutations (40-50%) are found in
KRAS and
BRAF [
23] and 17% of
PIK3CA mutations have been determined in colon carcinoma patients [
23,
24]. This suggests that the probability that a patient will not carry at least one of the above mentioned genetic changes is quite low. For this reason, HGUE-C-1 cells constitute an interesting and unique cellular model of colorectal carcinoma.
Since HGUE-C-1 cells were not obtained from the primary tumour when it was resected two years earlier, it becomes difficult to determine the initial events in carcinogenesis in this cellular model. Besides the loss of heterozygosity affecting the APC locus that we have found in HGUE-C-1 cells, we have studied different signal transduction pathways looking for modifications that we could associate with HGUE-C-1 tumourigenesis and, we have compared these results with the findings obtained in HT-29 colon cancer cells, since this cell line constitutes a paradigm of the colon carcinogenesis pathway proposed by Vogelstein et al. [
25]. HT-29 cells harbour
APC,
BRAF,
TP53 and
PIK3CA mutations and MSI stability. HGUE-C-1 cells expressed very low levels of Rb protein compared with HT-29 cells. These low levels of protein expression correlate with low activity of Rb protein and with increased activity of E2F, as demonstrated by transient transfection of both cell lines with the appropriate reporter genes (Figure
2). Our analysis also shows that HGUE-C-1 cells overexpress p70S6K (RPS6KB1), which correlates with an increased activity of this kinase, as demonstrated by its high level of phosphorylation under serum starved conditions and also because under the same conditions, its substrate RPS6 appears phosphorylated. Analysis of other signalling molecules that belong to the Ras/Raf/Mek/Erk and PI3K/Akt/mTOR pathways also shows some differences between both cell lines. Interestingly, Erk1 and Erk2 appear constitutively activated under serum starved conditions in HGUE-C-1 cells, as demonstrated by the high levels of Erk 1/2 phosphorylation. In addition, no expression of HER3 was observed in HGUE-C-1 cells. The results obtained open the possibility of a putative role of RPS6KB1 or Erk 1/2 as second hits in HGUE-C-1 carcinogenesis. Interestingly, several publications suggest that RPS6KB1 may be involved in carcinogenesis. Ehrbrecht et al. [
26] have analyzed 22 sporadic desmoplastic medulloblastomas by comparative genomic hybridization (CGH), finding in some of them an amplicon in chromosome 17 (17q22-24) where RPS6KB1 lies. Furthermore, they found significantly elevated transcript levels of RPS6KB1 as compared to normal cerebellum in 5 out of 6 desmoplastic medulloblastomas and in 4 out of 5 classic medulloblastomas analysed. The 17q23 amplicon has also been described by Sinclair et al. [
27] in breast cancer and they even have suggested that RPS6KB1, TBX2 and PPM1D genes included in this amplicon may act as oncogenes. Genetic variation in RPS6KA1, RPS6KA2, RPS6KB1 and RPS6KB2 has been related to colon and rectal carcinoma in a recent article by Slattery et al. [
28].
On the other hand, RPS6KB1 is regulated by growth factors such as EGF, PDGF and insulin, and is also regulated by mTOR [
29], suggesting that it can be involved in cell growth regulation. In this sense, Sunayama et al. [
30] have shown that inhibition of the PI3K/mTOR and the MEK/ERK pathways in glioblastoma stem-like cells induces an increase in the activity of the other pathways and that this cross-regulation disappeared when RPS6KB1 expression was inhibited by siRNAs. Using microarrays analysis, Chakraborty et al. [
31] identified genes related to tumourigenesis of retinoblastoma. Their results suggested that loss or inactivation of Rb lead to dysregulation of the PI3K/Akt/mTOR pathway. To corroborate this hypothesis, the authors reported an increase in the expression levels of PIK3CA, Akt, mTOR and RPS6KB1 in retinoblastoma samples, when compared with normal tissue. Taken together, these data suggested that loss of APC function and over-expression of RPS6KB1 in HGUE-C-1 cells alone or in combination with low activity and expression of Rb protein, may constitute a driving force in the HGUE-C-1 tumourigenesis.
HGUE-C-1 cells constitute a quite interesting model from a pharmacological point of view since they can be used for the study of intrinsic chemoresistance to 5-FU and irinotecan, as shown in Figure
3. Since chemoresistance was naturally acquired by the patient after treatment with these chemotherapeutic agents, these cells represent a more physiological model than the usual chemoresistance cellular models obtained in the laboratory by selective pressure of parental sensitive cells treated with increasing concentrations of a particular drug. In addition, clonal populations of HGUE-C-1 cells show different degrees of resistance to 5-FU. We need to investigate whether they represent different stages of a unique molecular mechanism of resistance or else, an alternative molecular mechanism of resistance developed inside the patient. Other possibility is that due to tumour heterogeneity, clonal populations behave differently under the same conditions.
HGUE-C-1 cells were also treated in culture with cetuximab, an antibody against the extracellular domain of EGFR, since as mentioned above, this is a treatment used in advanced colon carcinoma patients and since HGUE-C-1 cells are wild type for KRAS and BRAF. As seen in Figure
5A, HGUE-C-1 cells show resistance to cetuximab despite the patient was not treated with this antibody. Interestingly, HGUE-C-1 cells show sensitivity to erlotinib and gefitinib, small organic molecules that inhibit the tyrosine kinase activity of the EGFR. This is an unexpected result since cetuximab, erlotinib and gefitinib act against the same target (EGFR). Mutations on exons 19 and 21 of EGFR have been related to tyrosine kinase inhibitor activity [
32]. Since EGFR is expressed in HGUE-C-1 cells (Figure
3E), our results suggest that probably erlotinib and gefitinib act in HGUE-C-1 cells through the inhibition of a secondary target other than EGFR. Evidences showing inhibition of other tyrosine kinases by erlotinib and gefitinib have been previously published [
33].
In addition, the effect of several drugs affecting different signal transduction pathways have been analysed on HGUE-C-1 cells. Our results indicate that HGUE-C-1 cells show similar degree of sensitivity to rapamycin, NVP-BEZ235, sorafenib and TSA than HT-29 cells. These results indicate that inhibitors of the PI3K/mTOR pathway may be a therapeutic alternative for colon carcinoma patients with resistance to 5-FU, irinotecan, oxaliplatin and cetuximab. HGUE-C-1 cells are also sensitive to TSA (Figure
6D) and SAHA (data not shown), indicating that epigenetic treatments may be also a therapeutical alternative for these patients.
HGUE-C-1 cell proliferation was also inhibited by sorafenib. We can postulate that the effects of sorafenib could be due to the inhibition of BRAF, since HGUE-C-1 cells show wild type BRAF. However, we cannot conclude that this is the case since sorafenib also induces inhibition of HT-29 cell proliferation, and this cell line harbours a mutation in
BRAF (V600E) [
34]. We postulate that probably, the inhibitory effect of sorafenib is mostly due to its capacity to inhibit other tyrosine kinases [
35,
36], as it occurs with erlotinib and gefitinib.
The Hsp90 inhibitor 17-AAG is able to inhibit HGUE-C-1 cell proliferation, however, significant higher doses of 17-AAG are needed to inhibit HGUE-C-1 cells than HT-29 cells (Figure
7A). This partial response to 17-AAG may be related to the resistance of HGUE-C-1 cells to cetuximab. In this sense, it is believed that Hsp90 inhibitors affect cell proliferation because they interfere in the relationship between Hsp90 and their clients [
37]. Some of these clients are members of the HER family receptors [
38]. The lack of cetuximab effect may indicate that EGFR does not play a significant role in HGUE-C-1 cells and, in this sense, 17-AAG effects on HER family members could be no significantly important for HGUE-C-1 cell proliferation.
HGUE-C-1 cells also show resistance to AZD-6244 (selumetinib), a Mek inhibitor (Figure
7B). The molecular mechanisms involved in this resistance remain unknown. However, a putative explanation arises analysing the effects of the different drugs on cell cycle distribution, as seen in Figure
8. When we compare the effects of sorafenib, NVP-BEZ235, 17-AAG, AZD-6244 and TSA, we observed that in the case of HT-29 cells, the different drugs induce a partial blockade in different phases of the cell cycle and later, some percentage of the cells undergo apoptosis, as determined by an increase in the subG
1 population. However, this is quite different in HGUE-C-1 cells, since in this cell line, all drugs that affect cell proliferation induce directly an increase in the SubG
1 phase, without previous accumulation in any of the phases of the cell cycle. Even in the case of AZD-6244 treatment, where a very low and no significant effect on cell proliferation was observed, we could detect a small increase in the subG
1 cell population without any sign of cell accumulation in G
1, as opposed to the results obtained in HT-29 cells. Taking together, our data suggest that defects on the G
1/S checkpoint boundary in HGUE-C-1 cells due mainly to the low expression and activity of Rb, together with the increase on E2F activity (Figure
2C), are directly related to the lack of effect of AZD-6244 and to the partial effect of 17-AAG treatments in HGUE-C-1 cells.
Finally, HGUE-C-1 cells show resistance to oxaliplatin despite the patient was not treated with this compound. This resistance is important because as mentioned in the introduction, this compound increases survival in advanced colon carcinoma patients when added to the standard therapy with 5-FU or capecitabine and irinotecan [
5-
7]. The molecular mechanisms responsible for oxaliplatin resistance in HGUE-C-1 cells remain unknown. However, we believe that the low levels of Rb protein and activity may be involved in such mechanisms. Oxaliplatin damages the DNA inducing double strand breaks [
39]. Since HGUE-C-1 cells do not show MSI and express wild type
TP53, the expected response to oxaliplatin treatment in HGUE-C-1 cells should be p53 stabilization. Then, p53 will increase p21 and other proteins that will block the cell cycle in the G
1 phase. Since as we have shown the G
1/S checkpoint is seriously compromised by the low activity of Rb with the concomitant increase in E2F activity, HGUE-C-1 cells will be able to proliferate in such conditions. On the other hand, p53 will also increase the transcription of proapoptotic proteins such as NOXA and PUMA [
40] but again, HGUE-C-1 cells are able to survive in this conditions probably because as mentioned before, loss of Rb or decrease in its activity have been related to deregulation of PI3K/Akt/mTOR signal transduction pathway [
41]. This pathway has been extensively related with cell survival for example inhibiting the proapototic protein BAD [
42]. In this sense, it is interesting to mention that p70S6K that is constitutively active in HGUE-C-1 is able to phosphorylate BAD [
43].
Competing interests
The authors declare that they have no competing interests.
Authors’ contributions
Conceived and designed the experiments: PGM, JLS, IML, JGP, JAF, MS. Performed the experiments: SG, VMB, AC, TMB NLR. Analysed the data: VNB, JLS, JAF, MS. Wrote the paper: IML, PGM, MS. All authors read and approved the final manuscript.