Background
Cervical cancer is a major health problem worldwide; it is the second most frequent cause of cancer in women. An estimated 500,000 new cases, were reported in 2008, [
1], among which the most important was the presence of human papilloma virus (HPV) infection. High-risk HPV types 16 and 18 are responsible for > 70% of cases of cervix cancer [
2,
3].
Chemotherapy works in several ways. First, the cells die by apoptosis, which is an irreversible state defined as the genetically programmed cell death, consequently controlled by the balance between proapoptotic and antiapoptotic genes and characterized by cell shrinkage, membrane blebbing, chromatin condensation and nucleosomal DNA fragmentation. Apoptosis is the most convenient manner of tumor cell elimination, because this type of cell death is a final state and the tumor cell does not represent any possible future danger and does not induce inflammation [
4‐
6]. Other tumoral cell response to chemotherapy is the cellular senescence [
7]. This cellular state is considered a general biological program of permanent growth arrest and can be induced by telomere shortening (growing old) or by injuries to DNA such as those induced by chemotherapy which do not involve telomere shortening (accelerated senescence). In this state, the tumor cell cannot replicate. This was the reason it was considered originally as a protector mechanism against the development of neoplasia. However, recent data indicates that factors secreted by senescent cells can also alter the microenvironment, and enhance the tumor growth of neighboring tumor cells, indicating that this protective mechanism can act as a double-edged sword. Senescent cells exhibit changes in morphological characteristics such as enlarged and flattened cell shape and increased granularity. This distinction is identifiable with considerable specificity by the detection of β-galactosidase (SA-β-gal) through by X-gal activity staining [
8,
9].
The antitumor drug Cisplatin (CIS) with clinical and experimental efficiency is employed as a first-line chemotherapeutic modality in the treatment of epithelial malignancies, including lung, ovarian, testicular, cervix cancer and others [
10]. From a cell biology viewpoint, the principal mechanism of CIS-induced damage to tumors involves the interaction with DNA and activation of the mitogen-activated protein kinase (MAPK) signaling pathway, which controls a wide spectrum of cellular processes including growth, differentiation and apoptosis [
11].
Unfortunately, the chemotherapy's efficiency is so far from satisfactory due to the side effects and to the resistance of tumor cells. Recent publications open the possibility of increasing the efficiency of chemotherapy. Pentoxifylline (PTX), 1-[5-oxohexyl]-3, 7-dimethylxanthine] is a non-specific phosphodiesterase inhibitor that has been routinely employed for circulatory diseases for > 20 years. PTX is a potent inhibitor of tumor necrosis factor-alpha (TNF-α) and the transcription factor NF-κB. In this respect, our group reported that the 100% of lymphoma-bearing mice treated with PTX + adriamycin, an anthracycline, survived for > 1 year after receiving only one half of the therapeutic dosage of adriamycin. Similarly, we also observed that PTX increased the levels of apoptosis generated by adriamycin in fresh leukemic cells of pediatric patients [
12‐
14]. Sensitization of tumor cells to adriamycin by PTX is not tumor type specific. Similar results were observed in hematological and cervical cancer cell lines [
15].
The aim of this work was to investigate whether PTX can sensitize cervical cancer cells to apoptosis by means of CIS and modify cellular senescence. Our results indicate that in vitro, exposure of cervix tumor cells to PTX-treatment prior to CIS enhances apoptosis levels and reduces cell senescence.
Methods
Cell lines
HeLa (HPV-18+) and SiHa (HPV-16+) cervical cancer cell lines and the spontaneously immortalized human epithelial cell line HaCaT (used as non-tumorigenic control cells) were kindly provided by Dr. Boukamp (DKFZ-Heidelberg, Germany). The presence of the human papilloma virus (HPV) type was confirmed by the Linear array® genotyping test (Roche). All of the cell lines were maintained in vitro and propagated in Dulbecco's modified Eagle's culture medium (DMEM) supplemented with 10% heat-inactivated fetal bovine serum, 1X L-glutamine (2 mM final concentration) and antibiotics (penicillin/streptomycin). This medium will be referred to as DMEM-S, and was incubated at 37°C in an humidified atmosphere containing 95% air and 5% CO2. All of the previously mentioned products were obtained from GIBCO™ Invitrogen Corporation (Carlsbad, CA, USA).
Drugs and experimental conditions
Cisplatin (CIS) was obtained from PISA Laboratories, México, and stocked at 4°C for < 4 days and adjusted to a desirable concentration with DMEM culture medium immediately prior to utilization. Pentoxifylline (PTX) (Sigma Chemical Co., Saint Louis MO, USA) was dissolved in a sterile saline solution 0.15 M at a concentration of 0.2 M and maintained at 4°C < 4 days.
Cell culture and in vitrotreatments
HeLa, SiHa, and HaCaT cells suspended in DMEM-S at concentrations of 1.5 or 2 × 106 cells/8 mL in exponential phase were seeded in p100 Petri dishes for flow cytometry assays and senescence. For the survival test and for ELISA-determined apoptosis, the cells were cultured in 96-well plates at a concentration of 3 × 105 cells/well/200 μL (final volume). For clonogenic assays, the cells were seeded at densities of 1 × 104 cells/2 mL in 6-well plates. In all cases, the cells were cultured overnight at 37°C in a humidified atmosphere containing 5% of CO2 and 95% air. The medium was then replaced with DMEM-S. Then the cells were either treated with PTX 8 mM, or with CIS 4 μM or PTX + CIS (final concentrations). These doses of the individual drugs utilized were chosen base on the result of dose-response curves. These doses allow us to observe any further reductions caused by drug combination. The cells were incubated with PTX 1 hours prior to the addition of CIS and 24 hours later the culture cells were harvested. For gene expression study, the cells were incubated with the drugs for only 3 hours.
Clonogenic cell survival in vitro
Cells were assayed for the cytotoxic effects of PTX or CIS or PTX + CIS after cell survival according to the established methods of performing the clonogenic assay. Subconfluent cultures were exposed to the drugs for 6 hours. Then the cells were washed with PBS that was preheated to 37°C, trypsinized and plated in 6-well plates (100 cells/wells). After 15 days of incubation in complete culture medium, the colonies were stained with crystal violet after fixation with formaldehyde and were counted manually. In each case results are expressed as the survival fraction (SF), which was obtained by dividing the number of colonies formed after the treatment/number of cells seeded × PE. Plate efficiency (PE), PE = (
N
o
of colonies formed/
N
o
of cells seeded) × 100. Colonies (≥ 50 cells) usually appeared in 15 days. The number of colonies on control and drug-treated plates were counted on an inverted-stage microscope at 40-fold magnification. A minimum of 30 colonies/plate was required for an experiment to be considered evaluable for measurement of drug effect [
16].
Drugs interaction analysis
To determine the nature of the interaction between PTX and CIS, the data from the clonogenic assay were analyzed according to Chou and Talalay [
17] using CalcuSyn V2.0 software, (Biosoft, Cambridge, UK) [
18,
19]. For that, the drugs were combined at a constant ratio of PTX and CIS of 2000:1. The interaction of drugs was quantified determining a combination index (CI). CI < or > 1 indicated synergy or antagonism respectively, whereas a CI value of 1 indicates additivity [
20].
WST-1 assay
Cell survival was measured utilizing WST-1/ECS solution (BioVision Research, Mountain View, CA, USA). After 24 hours of incubation 10 μL/well of WST-1/ECS reagent was added and incubated for another 3 hours. Absorbance was measured on a microtiter plate reader (Synergy™ HT Multi-Mode Microplate Reader, Biotek Winooski, VT, USA) at 450 nm. Data are reported in percentage of cell survival as compared with the respectively untreated control group considered as 100%.
Early apoptosis and caspase activity detection methods
Cellular detection of annexin V, M30 (caspase -3,-6,-7 and-9) and caspase-8 activity was determined by flow cytometry employing the fluorescein isothiocyanate conjugated monoclonal annexin V-FITC apoptosis kit (annexin-V-FLUOS; Roche, Mannheim, Germany), M30 CytoDEATH™ Biotin antibody (Roche Mannheim, Germany), and the fluorescein active caspase-8 staining kit (Abcam, Cambridge, MA) respectively according to the manufacturer instructions. For the three tests at least 20,000 events were analyzed for each sample in an EPICS XL-MCL™ flow cytometer Beckman Coulter model (Fullerton, CA, USA). Data were processed with the System II software package (Beckman Coulter).
Apoptosis ELISA assays
In normal untreated and treated cell cultures, we determined cytoplasmic histone-associated-DNA-fragments (mono- and oligonucleosomes) spectrophotometrically (420 nm) utilizing Cell Death Detection ELISAPLUS (Roche Mannheim, Germany) according the manufacturer's instruction. Enrichment of mono- and oligonucleosomes released into the cytoplasm was calculated: experimental absorbance/corresponding control absorbance. The results are expressed as the percentage of DNA fragmentation.
Acridine orange/ethidium bromide staining to detect late apoptosis by Ultraviolet (UV)-microscopy
Briefly, the cells were stained, with ethidium bromide (Sigma Chemical Co. Saint Louis MO, USA) and acridine orange (Sigma Chemical Co. Saint Louis MO, USA) (100 μg/mL each). Two hundred cells were counted and the numbers of each of the following four cellular states were recorded: i) Live cells with normal nuclei (LN), bright green chromatin and organized structure; ii) Apoptotic cells (A) with highly condensed or fragmented bright green-yellow chromatin; iii) Dead cells with normal nuclei (DN), bright red chromatin and organized structure and iv) Dead cells with apoptotic nuclei (DA) and bright orange chromatin, which were highly condensed and fragmented. Apoptotic index (AI): A + DA/LN + A + DN + DA × 100 [
21].
β-galactosidase associated senescence
According to the manufacturer's instructions senescence was determined histochemically in treated and untreated control cells by Senescence Detection Kit (BioVision Mountain View, CA, USA) which detects β-galactosidase activity (SA-β-gal) present in senescence cells. We counted 300 cells of six microscopic fields to determine the percentage of SA-β-gal stained positive cells identified by an intense blue stain in the membrane.
15 × 106 cells were seeded in p150 culture Petri-dishes and treated next day with PTX, CIS and PTX + CIS for 24 hours. After treatment, cells were harvested by scraping and lysed with RIPA buffer (0.5% deoxycholate, 0.5% NP-40, 0.5% SDS, 50 mM Tris pH 7.4 and 100 mM NaCl) containing protein inhibitors. Following sonication (15 pulses, 90% amp), protein extracts were obtained after 30-min incubation at 4°C and 5-min centrifugation at 14,000 rpm/4°C. Protein concentrations were determined using BioRad DC Protein Assay Kit.
IκBα [pS32] and IκBα (total) ELISA
The levels of IκBα[pS32] and IκBα(total) protein were determined in HeLa and SiHa treated and untreated control cells employing a commercial ELISA kit (Invitrogen) at 450 nm according to the manufacturer's instructions. The results are expressed as optical density (O.D).
Bcl-2, Bcl-XL protein expression and phosphorylation state ERK1/2, p38 and p65 by flow cytometry
In normal untreated and treated cell cultures, we determinated the Alexa Fluor® 647mouse anti-human Bcl-2 and Alexa Fluor® 647 mouse anti human Bcl-XL proteins (Santa Cruz CA) and phosphorylated ERK1/2 (pT202/pY204) PE-Cy™7 mouse anti-human, Alexa Fluor® 488 mouse anti-human anti-phospho (P)-p38 (pT180/pY182) and Alexa Fluor® 647 mouse anti-human NF-κB p65 (pS529) BD Biosciences by flow cytometry. Cells were resuspended in PBS and stained according to protocol to detecting protein or activation of the phosphorylation state. An appropriate isotype control was utilized in each test to adjust for background fluorescence, and results are reported as Mean fluorescence intensity (MFI). For each sample, at least 20,000 events were acquired in a FACSAria-I cell sorter (BD Biosciences). Data were processed with the FACSDiva software (BD Biosciences).
Quantitative real time PCR
Total RNA from both types of cells was obtained after 3 hours of incubation using the PureLink™ Micro-to-Midi total RNA purification system (Invitrogen Corporation, Carlsbad, CA, USA). First-strand cDNA was synthesized from 5 μg of total RNA using Superscript™ III First-Strand Synthesis Supermix (Invitrogen Corporation, Carlsbad, CA, USA). Real Time PCR was performed using a LightCycler
® 2.0 apparatus (Roche Applied Science, Mannheim, Germany) and LightCycler-FastStart DNA Master
PLUS SYBR Green I (Roche Applied Science, Mannheim, Germany). Analysis of PCR products was performed using LightCycler
® software (Roche Applied Science, Mannheim, Germany). Data are expressed as relative quantities using a reference gene (Protein Ribosomal). Each sample was processed in triplicate to verify the specificity of the amplification reaction. Oligonucleotides (Invitrogen Corporation, Carlsbad, CA, USA) used to amplify human
IκBα, P65/RELA, BAD, BAK, BAX, NOXA, PUMA, P21, P53, P16, MCL-1, BCL-XL,
CASPASE-3, CASPASE-9, SURVIVIN, E6 and
E7 (HPV16 and
HPV18) and
L32 RIBOSOMAL PROTEIN are shown in Table
1. Oligonucleotides were designed using the Oligo V6 software. Gene sequences were obtained from the GenBank Nucleotide Database of the National Center for Biotechnology Information
http://www.ncbi.nlm.nih.gov.
Table 1
Primer pair sequences.
IκBα
| 5'GGA TAC CTG GAG GAT CAG ATT A 3' | |
| 5'CCA CCT TAG GGA GTA GTA GAT CAA T 3' | NM001278 |
P65/RELA
| 5'GCA GGC TCC TGT GCG TGT CT 3' | |
| 5'GGT GCT CAG GGA TGA CGT AAA G 3' | NM02975 |
BAD
| 5'CTC CGG AGG ATG AGT GAC GAGT 3' | |
| 5'ACT TCC GCC CAT ATT CAA GAT 3' | NM004322 |
BAK
| 5'CGC TTC GTG GTC GAC TTC AT 3' | |
| 5'AGA AGG CAA AGA CTT CGC TTA 3' | NM001188 |
BAX
| 5'TTT GCT TCA GGG TTT CAT CC 3' | |
| 5'CAG TTG AAG TTG CCG TCA GA 3' | NM138764 |
NOXA
| 5'GAG ATG CCT GGG AAG AAG G 3' | |
| 5'TCC TGA GCA GAA GAG TTT GGA 3' | NM021127 |
PUMA
| 5' GAT GGC GGA CGA CCT CAA C 3' | |
| 5'TGG GAG TCC AGT ATG CTA CAT GGT 3' | NM014417 |
P21
| 5'CGA CTT TGT CAC CGA GAC AC 3' | |
| 5'CGT TTT CGA CCC TGA GAG T 3' | NM000389 |
P53
| 5'CTG AGG TTG GCT CTG ACT GTA CCA CCA TCC 3' | |
| 5'CTC ATT CAG CTC TCG GAA CAT CTC GAA GCG 3' | NM000546 |
P16
| 5'CAG TAA CCA TGC CCG CAT AGA T 3' | |
| 5'TGA AAA GGC AGA AGC GGT GT 3' | NM000077 |
MCL-1
| 5'CAC GAG ACG GTC TTC CAA GGA TGC T 3' | |
| 5'CTA GGT TGC TAG GGT GCA ACT CTA GGA 3' | NM021960 |
BCL-
XL
| 5'GCA GGC GAC GAG TTT GAA CT 3' | |
| 5'GTG TCT GGT CAT TTC CGA CTG A 3' | NM138578 |
CASPASE 3
| 5'ATA CTC CAC AGC ACC TGG TTA T 3' | |
| 5'AAT GAG AGG GAA ATA CAG TAC CAA 3' | NM004346 |
CASPASE 9
| 5'GTA CGT TGA GAC CCT GGA CGA C 3' | |
| 5'GCT GCT AAG AGC CTG TCT GTC ACT 3' | NM001229 |
SURVIVIN
| 5'TGA GCT GCA GGT TCC TTA TCT G 3' | |
| 5'GAA TGG CTT TGT GCT TAG TTT T 3' | NM001168 |
DIABLO
| 5'TGA CTT CAA AAC ACC AAG AGT A 3' | |
| 5'TTT CTG ACG GAG CTC TTC TA 3' | NM019887 |
E6 (HPV 18)
| 5'GCG ACC CTA CAA GCT ACC TGA T 3' | |
| 5'GCA CCG CAG GCA CCT TAT TA 3' | X05015 |
E7 (HPV 18)
| 5'TGT CAC GAG CAA TTA AGC GAC T 3' | |
| 5'CAC ACAAAG GAC AGG GTG TTC A 3' | X05015 |
E6 (HPV 16)
| 5'CAG AGC TGC AAA CAA CTA TAC 3' | |
| 5'AGT GGC TTT TGA CAG TTA ATA C 3' | NC001526 |
E7 (HPV 16)
| 5'GAC AAG CAG AAC CGG ACA G 3' | |
| 5'ATT CCT AGT GTG CCC ATT AAC A 3' | NC001526 |
L32 RIBOSOMAL
| 5'GCA TTG ACA ACA GGG TTC GTA G 3' | |
PROTEIN
| 5'ATT TAA ACA GAA AAC GTG CAC A 3' | NM000994 |
Statistical analysis
Results of each experiment represent the means ± standard deviation (SD) of three independent experiments carried out in triplicate. Student's t-test was used for statistical analyses a value of P < 0.05 was considered significant. For the comparison of gene expression was considered as significant differences values of ≥ 30%. In some cases was calculated the Δ% that represent the percent of increment or diminution in relation to comparative group.
Discussion
In the present work, we found good correlation between survival and different apoptotic assays. Surprisingly, PTX per se results toxic for HeLa and SiHa tumor cells and sensitizes these to the toxic action of CIS, increasing apoptosis and simultaneously reducing senescence. It is also noteworthy that as an advantage, PTX is more toxic than CIS in cancer cells and was practically not toxic for non-tumorigenic HaCaT keratinocytes.
We detected early and late apoptosis because in the first steps apoptosis can be reversible [
22]. The UV light microscopy test allowed us to appreciate a definitive status. The observation that non-tumorigenic HaCaT cells are less sensitive to different treatments is probably due to the fact that the rate of multiplication and metabolism is slower in HaCaT cells than in tumor cells.
These results are in agreement with other published data reporting that PTX sensitizes
in vivo and
in vitro cancer cells to chemotherapy, particularly to adriamycin [
12]. Within this context, we previously reported that the PTX is able to sensitize lymphoma and leukemic cancer cells to apoptosis by adriamycin or perillyl alcohol [
13]. Similar results have been reported with radiotherapy [
23]. The observations of the present work are in agreement with recent data in which our group demonstrated that PTX increases apoptosis and inhibits senescence in HeLa and SiHa Cells treated with adriamycin, an anthracycline used also against cervical cancer [
15]. The present results are important because CIS is the first drug of election in the treatment of cervical cancer. Additionally to published data, the results of the present work strongly suggest that the cytotoxicity of PTX is not limited to one type of tumor cells or to chemotherapeutic drugs, incrementing its potential utilization in Oncology.
The low toxicity showed by CIS in survival test may be explained because CIS induces senescence. Senescence originally was considered to be a tumor-suppressor mechanism [
24,
25]. However its role in Oncology is not clear because senescent cells though they cannot replicate, continue releasing growth factors, enzymes and other products that under certain conditions promote tumor growth [
9,
26]. It is very interesting that PTX does not induce senescence, and strongly decreases the senescence induced by CIS. The importance of these observations is that an antitumoral treatment that induces principally apoptosis rather than senescence is preferable in cancer cells.
Different mechanisms can explain our observations. PTX also has antimetastatic activity [
27] and arrests the cell cycle in the G2/M, in which the tumors are more sensitive to the toxic effects of some chemotherapeutic and radiotherapeutic agents [
28,
29]. PTX has been linked as well to the activation of caspase [
12,
30]. In this study, an important activity of caspase (-3, -6 -7 -9 and -8) was detected in HeLa and SiHa cells treated with PTX or PTX + CIS and, in minor degree, with CIS. In addition, this caspase activity is directly proportional to the level of apoptosis confirming its participation. In SiHa cells treated with CIS alone, we observed low caspase activity. In this regard, it has been reported that CIS may also exert its apoptotic activity by caspase-independent pathways [
31].
PTX is a strong inhibitor of phosphodiesterase activity. In murine lymphoma and U937 human monocyte cell line, it also prevents activation NF-κB in these cells [
12] by inhibition of the phosphorylation of serine 32 in IκB complex. Thus preventing TNF-α secretion and expression of certain antiapoptotic genes that possess antioxidant activity [
32]. Contrariwise, CIS promotes the formation of reactive oxygen species (ROS), which provoke apoptosis or senescence [
33].
We also studied the phosphorylation of different proteins that are important for proliferation, differentiation, cell survival, apoptosis and senescence such as ERK1/2 and p38 from the family of mitogen activated protein kinases (MAPKs) and phosphorylation of the p65 subunit of NF-κB and related IκB proteins. Induction of death by CIS has been associated with increase in p38 and ERK1/2 activity [
11,
34]. We observed this activity in SiHa and HeLa cells, but it has been demonstrated that ERK1/2 activity induced by CIS can cause resistance in SiHa cells [
35], gastric cancer cells [
36], and human myeloid leukemic cells [
37]. PTX decrease ERK1/2 phosphorylation in SiHa cells, this disrupts resistance to CIS, because when we utilized PTX, apoptosis was higher than in CIS-treated cells. Is it noteworthy that, PTX decreased the phosphorylation of p65 and IκBα (S32), thus resulting in the inhibition of nuclear translocation of NF-κB and avoiding the cell survival and resistance observed in CIS-treated cells [
38‐
40]. NF-κB can activate different genes related with the cell survival such as Bcl-2 and Bcl-XL [
41]. It's important to stress that PTX by itself or in combination with CIS disrupt the NF-κB pathway. We observe an inhibition of phosphorylation the IκBα, p65 and decrease the levels of anti-apoptotic proteins Bcl-2 and Bcl-XL in HeLa and SiHa cells. This is important because these antiapoptotic proteins confer resistance to several chemotherapeutic agents including CIS, gemcitabine, vincristine, etoposide, doxorubicin, and paclitaxel [
42].
In our study, PTX significantly disrupted the CIS resistance in HeLa and SiHa cell by blocking the NF-κB mediated survival pathway. PTX possesses an additive effect with CIS (8 mM + 4 μM respectively); the combined usage of these two drugs promotes apoptosis of cervical tumor cells and at the same time impairs senescence.
Our results suggest that PTX action on NF-κB, ERK1/2, p38, Bcl-2 and Bcl-XL proteins and caspases can explain the fact that it does not induce senescence, but does increase apoptosis in HeLa and SiHa cells. In addition, when we employed PTX in combination with CIS, it impaired CIS-induced senescence and increased the sensitivity of these cervix cancer cells to this drug. Therefore, we think that PTX could be used to abrogate NF-κB-induced resistance mechanisms without severe systemic toxicity. Thus, the use of PTX with other chemotherapeutic agents such as CIS may lead to more efficient cervical cancer cell elimination.
Moreover, a gene expression analysis to study the antitumoral effects of drugs is critical in order to identify the potential PTX + CIS-specific genetic targets involved. Employing an RT-PCR assay, we studied the mRNA expression of genes related NF-κB pathway, apoptosis and senescence. In general, we observed in HeLa and SiHa cervix cancer cells an up-regulation of some proapoptotic genes after PTX + CIS treatment, including the DIABLO, NOXA, PUMA, CASPASES-3 and -9 genes, which are implicated in the mitochondrial pathway of apoptosis [
43]. It is noteworthy that treatment with CIS induces the expression of anti-apoptotic gene, SURVIVIN. These phenomena have been reported as another cause of tumor-cell resistance to chemotherapy [
44,
45]. Up-regulation of SURVIVIN is also present in senescent tumor cells. To the contrary, treatment with PTX alone in all experimental groups, down-regulated the expression of SURVIVIN gene. These results show that PTX can overcome one of the survival strategies used by the cancer cells in response to chemotherapeutic agents. The Bcl-2 family genes protect the cells of CIS-induced apoptosis [
46,
47]. This fact contributes to the explanation of all our results because we found that some survival genes are down-regulated by PTX, as it the case with BCL-
XL. The strongly over-expression of some pro-apoptotic genes likes PUMA (4500%), tip the balance in favor of apoptosis. CIS administration paradoxically leads to an antiapoptotic effect of p53 pathway, which induces tumor cell resistance to CIS [
48,
49]. In our work, we demonstrated that PTX counteracts this effect by promoting apoptosis in HeLa and SiHa cells, as confirmed by the over-expression of PUMA, NOXA and P21 genes which are regulated by p53 [
50]. This does not exclude the existence of other p53-independent pathways for induction of apoptosis, because we found a slight over-expression of P53 compared with the high over-expression of NOXA, PUMA and P21 genes [
51‐
53]. It is important to remark that these results together agree with the direct determination of the most important proteins related with apoptosis and the cell survival under our experimental conditions. The senescence-associated P16 gene, exhibits a different behaviour between two cancer cervix lines. CIS induced up-regulation of the P16 gene in HeLa and SiHa cancer cells, is incomplete accordance to the senescence levels observed in β-galactosidase assay in these cells.
With regard to IκBα and P65/RELA genes, related to transcription factor NF-κB, IκBα and P65 expression, were down-regulated or remained unchanged with all treatments in SiHa cells, suggesting a diminution of the availability of these factors, which facilitate cell apoptosis. However, in the three treated groups of HeLa cells, we observed an up-regulation of IκBα and P65/RELA genes strictly that was comparable between these genes suggesting an equal balance of both factors.
In the non-tumorigenic line HaCaT we observed a different behaviour in comparison with cervical tumor cells. In general, we noted an important activation of genes with proapoptotic activity, including BAB, BAX, NOXA and P21 (CIS and PTX + CIS), as well as in PTX groups for CASPASE-3 gene. However, despite of the up-regulation of several proapoptotic genes, apoptosis levels were low and cell viability was not affected, suggesting that the rate of multiplication displays an important effect in the action of the assayed drugs. In this respect, is also important to mention that P65 is up-regulated > 7-fold and BCL-XL 5-fold, and we found no important levels of apoptosis.
Because expression of mRNA E6/E7 genes appear to play a key role in cervical cancer development, we conducted an analysis in human cervical carcinoma SiHa and HeLa cell line. We observed a decrease in the expression of E6 and E7 genes only in SiHa cells, treated with the different drugs, although in HeLa cells we observed no effect on these genes. In both cancer cell lines, we observed induction apoptosis and sensibilization by PTX. This indicates that several mechanisms of resistance and susceptibility to antitumoral drug could be implicated, such as the HPV types and their interactions with the cells.
The choice between survival, senescence or apoptosis, is a very complex process [
54,
55]. Rather than the action of a single gene or molecules, the final balance between activation or not of these genes and molecules determines whether or not a cell undergoes apoptosis. In this study, we observed an overall balance in favor of the apoptotic process in HeLa and SiHa cancer cells treated with PTX and/or CIS.
Authors' contributions
GHF, ABC, PCOL designed and performed the research, analyzed the data and drafted the manuscript; JMLD, JRDR, YCC and RCC performed some of the research and analyzed the data, AAL, LFJS and STA performed molecular study. All the authors read and approved the final manuscript