Open Access

Combination of BCL11A siRNA with vincristine increases the apoptosis of SUDHL6 cells

European Journal of Medical Research201419:34

https://doi.org/10.1186/2047-783X-19-34

Received: 18 April 2014

Accepted: 11 June 2014

Published: 24 June 2014

Abstract

Background

B cell chronic lymphocytic leukemia/lymphoma 11 A (BCL11A) is associated with human B cell malignancy initiation. Our previous study has shown that downregulation of BCL11A mRNA by small interfering RNA (siRNA) is capable of inducing apoptosis in the SUDHL6 cell line. To further explore the effects of BCL11A siRNA on the enhanced cytotoxicity of a chemotherapeutic drug, we investigated the effects of BCL11A siRNA combined with vincristine (VCR) on SUDHL6 cell proliferation and apoptosis.

Methods

Chemically synthesized BCL11A siRNA was transfected into SUDHL6 cells using the HiPerFect Transfection Reagent in combination with VCR. Cell proliferation was measured by the CCK8 assay. The morphology of apoptotic cells was observed with Hoechst 33258 staining. The rate of cell apoptosis was determined by annexin V-fluorescein isothiocyanate/propidium iodide double staining using fluorescence-activated cell sorting (FACS) analysis.

Results

After BCL11A siRNA plus VCR treatment, cell proliferation was significantly decreased in comparison with VCR or BCL11A siRNA treatment alone and negative control siRNA plus VCR treatment (P <0.05). The apoptotic rate of BCL11A siRNA plus VCR treated cells was significantly increased compared with BCL11A siRNA and VCR treatment alone and negative control siRNA plus VCR treatment (P <0.05).

Conclusions

The combination of BCL11A siRNA and VCR increases apoptosis in SUDHL6 cells. Our study implies that BCL11A siRNA in combination with VCR may be a useful approach for improving effective treatment for B cell lymphoma.

Keywords

BCL11A small interfering RNA vincristine SUDHL6 cells apoptosis

Background

Diffuse large B cell lymphoma (DLBCL) is the most common type of non-Hodgkin lymphoma (NHL)[1, 2]. DLBCL is a heterogeneous disease in its morphology, immunophenotype, and biological behavior, and it includes subtypes with diverse origins and gene expression profiles[1, 3]. Current treatments for NHL are not optimally effective and mainly result in relapse and resistance to chemotherapy[4, 5]. Therefore, further investigation of specific DLBCL biomarkers, development of more targeted treatments, and improvement of the effects of treatment are indispensable for significantly increasing the survival of patients.

B cell chronic lymphocytic leukemia/lymphoma 11 (BCL11) gene family members, including the BCL11A and BCL11B, have been identified as transcriptional repressors, which are essential for lymphoid development[68]. The BCL11B gene, which is related to malignant T cell transformation, plays a crucial role in the development, proliferation, differentiation and subsequent survival of T cells[9]. BCL11A has been identified on human chromosome 2p16.1 (previously mapped at 2p13) where chromosomal abnormalities are associated with human lymphoma[10, 11]. Recently, Yin et al. suggested that BCL11A acts as an oncogene and may contribute to leukemogenesis in certain groups of AML patients[12]. BCL11A overexpression is primarily found in B cell lymphoma and B cell leukemia[11, 1316]. We and others have demonstrated the essential role of BCL11A in the proliferation and survival of B cells[8, 17]. Our previous study has shown that downregulation of BCL11A mRNA by small interfering RNA (siRNA) is capable of inducing apoptosis in B lymphoma cell lines (SUDHL6 and EB1)[17]. Gene expression profiling revealed that various genes related to apoptosis and proliferation are altered during BCL11A siRNA-mediated SUDHL6 cell apoptosis (WH and Gao Yangjun, unpublished data).

Vincristine (VCR) is a commonly used chemotherapeutic agent for many lymphoid malignancies, including aggressive NHL. Depending on the therapeutic dose, most chemotherapeutic agents have side effects. VCR has additional peripheral neurological side effects such as hearing changes, sensory loss, numbness, and tingling[18]. Serious side effects in response to chemotherapeutic agents led researchers to seek novel anticancer agents with fewer side effects, and these newly explored anticancer agents can be used in combination with commonly used chemotherapeutic agents to reduce serious side effects[1922]. A recent report suggested a possible synergy between VCR and the amino acid-depleting agent pegylated arginase I (BCT-100) in treating T-ALL in the cancer microenvironment[23].

RNA interference (RNAi)-based therapeutics has emerged for the treatment of various human diseases including cancer[22, 24]. Based on the efficacy of BCL11A siRNA in inhibiting SUDHL6 cells[17], we hypothesized that BCL11A siRNA plus VCR enhances inhibitory activity in SUDHL6 cells. To the best of our knowledge, our findings indicate for the first time that BCL11A siRNA increases VCR-induced apoptosis in SUDHL6 cells. Therefore, our study implies that the combination of BCL11A siRNA transfection plus VCR is an efficacious therapeutic approach for treating B cell lymphomas that express BCL11A.

Methods

Reagents

BCL11A-specific siRNA (sense: GAAUCUACUUAGAAAGCGATT and antisense: UCGCUUUCUAAGUAGAUUCTT, Chinese patent number: ZL 2011 1 0301731.6), which targets domains in the third exon of the BCL11A gene (ACCESSION NM_022893.3), [EMBL:AJ404611], and its corresponding non-silencing negative control siRNA were designed and synthesized by Shanghai GenePharma Co., Ltd. (Shanghai, China). RPMI 1640 and newborn calf serum were purchased from Gibco (Gibco, Carlsbad CA, USA). VCR was purchased from Shenzhen Main Luck Pharmaceuticals, Inc (Shenzhen, Guangdong, China).

Cell culture and transfection

The SUDHL6 cell line, which was derived from germinal center B cell-like DLBCL, was kindly provided by Professor Ailin Guo from the Department of Pathology (Cornell University, Ithaca, NY, USA). The cells were cultured in RPMI medium supplemented with 10% heat-inactivated fetal calf serum at 37°C under 5% CO2 in a humidified incubator. SUDHL6 cells in the exponential growth phase were grown for 24 hours and then transfected using HiPerFect (Qiagen, Valencia, CA, USA) according to the manufacturer’s protocols. In addition, cells were transfected with negative control siRNA. The total concentration of siRNA applied in every case was maintained constant at 100 nM.

Assay of cell viability

For the quantitative determination of cellular proliferation and viability, we performed the CCK8 assay. This assay was performed after SUDHL6 cells were transfected with BCL11A siRNA in combination with VCR (1 μM) at 24, 48 and 72 h. The cells were washed, counted and seeded at a density of 4 × 105 cells/ml per well in 96-well plates. Six hours later, BCL11A siRNA in combination with VCR was added to the cells. At 48 and 72 h after transfection, CCK8 solution was added 4 h before the end of incubation. Cell viability was measured with a spectrophotometer at an absorbance of 450 nm. The inhibition rates of cell growth were calculated according to the following formula: inhibition rate (%) = (1 ‒ mean absorbance of treatment group/mean absorbance of untreatedmentgroup) × 100%.

Assays of cell apoptosis

Transfected SUDHL6 cells were harvested after treatment. Morphology was determined with Hoechst 33258 following incubation for 72 h. Cells were washed with PBS three times and then stained with 10 μl Hoechst33258 nuclear dye (KeyGEN, Nanjing, China) for 10 min at 37°C. After cells had been washed with PBS three times, images were obtained with a fluorescence microscope (Leica, Germany). Apoptosis assays were performed using annexin V-fluorescein isothiocyanate (annexin V-FITC) and propidium iodide (PI) (BD Pharmingen, San Jose, CA, USA) according to the instructions of the manufacturer. Briefly, cells were centrifuged, washed with cold PBS, and then resuspended in 500 μl binding buffer. FITC-conjugated Annexin V (10 μl) and PI (10 μl) were added to each sample, and the mixture was incubated at 4°C in the dark for 5 min. The cells were then immediately subjected to fluorescence-activated cell sorting (FACS) analysis (BD FACS Calibur, Franklin Lakes, New Jersey, USA). The percentage of early and late apoptotic cells in each group was determined.

Statistical analysis

Results are shown as the mean ± s.d. Statistical comparisons were made using ANOVA. Differences were deemed significant for a real alpha of 0.05. All statistical analysis was performed with SPSS 13.0.

Results and discussion

BCL11A is a Krüppel-like transcription factor that is closely related to B cell proliferation and differentiation[6, 8]. High expression of BCL11A is thought to possibly be involved in the genesis of B cell neoplasms[11, 1316]. We found that downregulation of BCL11A expression by siRNA can inhibit proliferation and induce apoptosis in SUDHL6 cells[17]. Gene expression profiling of BCL11A siRNA-treated SUDHL6 cells in our laboratory also highlighted that BCL11A might be related to a variety of signaling networks including apoptosis and the cell cycle (WH and Gao Yangjun, unpublished data). In this study, consistent with our previous report, BCL11A siRNA inhibited the proliferation and growth of SUDHL6 cells[17]. These results suggest that oncogenic BCL11A may be a rational therapeutic target in B cell lymphoma. Hence, of particular interest is to observe whether BCL11A siRNA significantly enhances the therapeutic efficacy of chemotherapeutic drugs in B cell malignancy. Therefore, we attempted to explore the combinatorial effects of BCL11A siRNA and a chemotherapeutic agent (VCR).

Interestingly, our results demonstrated that cell viability was more effectively reduced by BCL11A siRNA combined with VCR in a time-dependent fashion (P <0.05) (Figure 1). Furthermore, in order to identify the mechanism responsible for this decline in cell viability, a morphology assay was used. Our results showed significant apoptotic morphology changes such as chromatin condensation and fragmentation at 72 h after transfection with BCL11A siRNA in combination with VCR in SUDHL6 cells (Figure 2). Moreover, there was a large increase in annexin V- FITC/PI double-positive cells at 72 h after transfection with BCL11A siRNA in combination with VCR in SUDHL6 cells. The apoptosis rate of BCL11A siRNA combined with VCR treatment was (71.46 ± 2.53)%, which was statistically significantly different compared with BCL11A siRNA (39.64 ± 5.17)% or VCR (49.73 ± 6.74)% treatment alone (P <0.05) (Figure 3). There was no significant difference compared with VCR and the negative control siRNA plus VCR treatment (50.32 ± 6.18)%. Therefore, this study showed that BCL11A siRNA in combination with VCR enhances apoptosis, thereby inhibiting the proliferation and growth of SUDHL6 cells. These results indicate that there is a potential therapeutic benefit for the combination of BCL11A siRNA and VCR compared with BCL11A siRNA or VCR alone.
Figure 1

The rate of inhibition of SUDHL6 cell growth as measured by the CCK8 assay after combined treatment with BCL11A siRNA plus vincristine (VCR). SUDHL6 cell proliferation was determined by the CCK8 assay. The inhibition rates for cell growth were calculated according to the following formula: inhibition rate (%) = (1 - mean absorbance of treatment group/mean absorbance of untreated group) × 100%, and the resulting values were plotted. The results represent mean values from three independent experiments ± s.d.

Figure 2

The morphology effects from the combination of BCL11A siRNA plus vincristine in SUDHL6 cells at 72 hours. The nuclear morphology of cells stained with Hoechst 33258 was analyzed by fluorescence microscopy (400×) at 72 h after transfection. Data are representative microscopic images of three independent experiments. A) untreated cells; B) negative control siRNA; C) BCL11A siRNA; D) vincristine; E) negative control siRNA plus vincristine; F) BCL11A siRNA plus vincristine.

Figure 3

The rate of apoptosis induced by the combination of BCL11A siRNA and vincristine in SUDHL6 cells at 72 hours. Apoptosis was analyzed by annexin V-FITC/PI staining 72 h after treatment. Data are representative images of three independent experiments. A) untreated cells; B) negative control siRNA; C) BCL11A siRNA; D) vincristine; E) negative control siRNA plus vincristine; F) BCL11A siRNA plus vincristine.

These results are consistent with a related report that showed that silencing the antiapoptotic protein Bfl-1 by siRNA in DLBCL cell lines induced apoptosis and sensitized those cells to apoptosis induced by chemotherapeutic compounds such as doxorubicin, vincristine, cisplatin and fludarabine[25].

SUDHL6 cells, which were chosen for this study, are characterized by a t(14;18) chromosomal translocation resulting in overexpression of the antiapoptotic protein BCL-2. In SUDHL6 cells transfected with BCL11A siRNA, we found that the apoptosis gene BIM (BCL2-interacting mediator of cell death) was upregulated, and the anti-apoptosis genes BCL-2 and MDM2 (murine double minute 2) were downregulated (WH and Gao Yangjun, unpublished data). A recent study has suggested BCL11A deletion causes apoptosis in early B cells in vivo and in vitro by directly regulating BCL-2, BCL-xL, MDM2, and MDM4[8].

Two research groups demonstrated that the small molecule ABT-737, a BCL-2 homology domain 3 mimetic, in combination with VCR increased the apoptotic cell death of leukemia cell lines[26, 27]. Our previous studies and other groups have suggested that downregulation of BCL-2 expression by siRNA increases the sensitivity of human tumor cells to chemotherapeutic drugs[2830]. MDM2 negatively regulates the activity of the tumor suppressor protein p53, thus having an anti-apoptotic role[31]. MDM2 inhibition by the antagonist nutlin-3 sensitizes neoplasm cells to chemotherapy-induced apoptotic cell death[32, 33]. The mechanism of induced apoptosis mediated by VCR is complex and involves protein kinase signaling pathways[34]. Mitochondria also appear to play a key role in this process[35]. Based on these findings, we inferred that the BCL11A siRNA plus VCR-induced apoptosis of SUDHL6 cells might be related to the downregulation of BCL-2 and MDM2 and upregulation of BIM. However, how BCL11A siRNA and VCR are involved in enhancing the apoptotic process by BCL-2, MDM2 and/or BIM needs further investigation.

Conclusions

We demonstrated that combined treatment with BCL11A siRNA and VCR increases the inhibitory effects of in vitro cell growth and apoptosis in SUDHL6 cells. Our study indicates that the combination of BCL11A siRNA and VCR offers a novel and potential therapeutic strategy for B cell malignancies. However, further investigation of a wide range of B lymphoma cell types and chemotherapeutic drugs and in vivo studies confirming the efficacy of this treatment paradigm are necessary.

Abbreviations

BCL11A: 

B cell chronic lymphocytic leukemia/lymphoma 11A

BIM: 

BCL2-interacting mediator of cell death

DLBCL: 

diffuse large B cell lymphoma

FACS: 

fluorescence-activated cell sorting

FITC: 

fluorescein isothiocyanate

GCB: 

germinal center B cell-like

MDM2: 

murine double minute 2

NHL: 

non-Hodgkin lymphoma

PI: 

propidium iodide

RNAi: 

RNA interference

siRNA: 

small interfering RNA

VCR: 

vincristine.

Declarations

Acknowledgements

We thank senior experimentalist Lijian Yang (Medical College, Jinan University, Guangzhou) for kindly providing valuable technical support and advice. This project was supported by grants from the National Natural Science Foundation of China (No. 91129720), the Guangdong Province Key Foundation of Science and Technology Program (2009B0507000029, 2012B050600023) and a grant from the Overseas Chinese Affairs Office of the State Council Key Discipline Construction Fund (51205002).

Authors’ Affiliations

(1)
Institute of Hematology, Medical College, Jinan University
(2)
Key Laboratory for Regenerative Medicine of Ministry of Education, Jinan University

References

  1. Küppers R: Mechanisms of B-cell lymphoma pathogenesis. Nat Rev Cancer 2005, 5: 251–262.PubMedView ArticleGoogle Scholar
  2. Sabattini E, Bacci F, Sagramoso C, Pileri SA: WHO classification of tumours of haematopoietic and lymphoid tissues in 2008: an overview. Pathologica 2010, 102: 83–87.PubMedGoogle Scholar
  3. Tirado CA, Chen W, García R, Kohlman KA, Rao N: Genomic profiling using array comparative genomic hybridization define distinct subtypes of diffuse large B-cell lymphoma: a review of the literature. J Hematol Oncol 2012, 5: 54.PubMedPubMed CentralView ArticleGoogle Scholar
  4. Johnston PB, Yuan R, Cavalli F, Witzig TE: Targeted therapy in lymphoma. J Hematol Oncol 2010, 3: 45.PubMedPubMed CentralView ArticleGoogle Scholar
  5. Steinhardt JJ, Gartenhaus RB: Promising personalized therapeutic options for diffuse large B-cell Lymphoma Subtypes with oncogene addictions. Clin Cancer Res 2012, 8: 4538–4548.View ArticleGoogle Scholar
  6. Liu P, Keller JR, Ortiz M, Tessarollo L, Rachel RA, Nakamura T, Jenkins NA, Copeland NG: Bcl11a is essential for normal lymphoid development. Nat Immunol 2003, 4: 525–532.PubMedView ArticleGoogle Scholar
  7. Li L, Leid M, Rothenberg EV: An early T cell lineage commitment checkpoint dependent on the transcription factor Bcl11b. Science 2010, 329: 89–93.PubMedPubMed CentralView ArticleGoogle Scholar
  8. Yu Y, Wang J, Khaled W, Burke S, Li P, Chen X, Yang W, Jenkins NA, Copeland NG, Zhang S, Liu P: Bcl11a is essential for lymphoid development and negatively regulates p53. J Exp Med 2012, 209: 2467–2483.PubMedPubMed CentralView ArticleGoogle Scholar
  9. Huang X, Du X, Li Y: The role of BCL11B in hematological malignancy. Exp Hematol Oncol 2012, 1: 22.PubMedPubMed CentralView ArticleGoogle Scholar
  10. Küppers R, Sonoki T, Satterwhite E, Gesk S, Harder L, Oscier DG, Tucker PW, Dyer MJ, Siebert R: Lack of somatic hypermutation of IG V(H) genes in lymphoid malignancies with t(2;14)(p13;q32) translocation involving the BCL11A gene. Leukemia 2002, 16: 937–939.PubMedView ArticleGoogle Scholar
  11. Satterwhite E, Sonoki T, Willis TG, Harder L, Nowak R, Arriola EL, Liu H, Price HP, Gesk S, Steinemann D, Schlegelberger B, Oscier DG, Siebert R, Tucker PW, Dyer MJ: The BCL11 gene family: involvement of BCL11 A in lymphoid malignancies. Blood 2001, 98: 3413–3420.PubMedView ArticleGoogle Scholar
  12. Yin B, Delwel R, Valk PJ, Wallace MR, Loh ML, Shannon KM, Largaespada DA: A retroviral mutagenesis screen reveals strong cooperation between Bcl11a overexpression and loss of the Nf1 tumor suppressor gene. Blood 2009, 113: 1075–1085.PubMedPubMed CentralView ArticleGoogle Scholar
  13. Liu H, Ippolito GC, Wall JK, Niu T, Probst L, Lee BS, Pulford K, Banham AH, Stockwin L, Shaffer AL, Staudt LM, Das C, Dyer MJ, Tucker PW: Functional studies of BCL11A: characterization of the conserved BCL11A-XL splice variant and its interaction with BCL6 in nuclear paraspeckles of germinal center B cells. Mol Cancer 2006, 5: 18.PubMedPubMed CentralView ArticleGoogle Scholar
  14. Weniger MA, Pulford K, Gesk S, Ehrlich S, Banham AH, Lyne L, Martin-Subero JI, Siebert R, Dyer MJ, Möller P, Barth TF: Gains of the proto-oncogene BCL11A and nuclear accumulation of BCL11A(XL) protein are frequent in primary mediastinal B-cell lymphoma. Leukemia 2006, 20: 1880–1882.PubMedView ArticleGoogle Scholar
  15. Gao Y, He D, Chen S, Yan X, Hu X, Li Y: Quantitative detection of BCL11A gene expression B cell malignancies by real-time RT-PCR. J Jinan Univ Med Ed 2011, 32: 147–150. (In Chinese)Google Scholar
  16. Gao Y, He D, Chen S, Yan X, Hu X, Li Y: Expression of the B-cell lymphoma/leukemia BCL11A gene in malignant hematological cell lines through quantitative reverse transcription polymerase chain reaction. Clin Oncol Cancer Res 2011, 8: 242–246.View ArticleGoogle Scholar
  17. Gao Y, Wu H, He D, Hu X, Li Y: Downregulation of BCL11A by siRNA induces apoptosis in B lymphoma cell lines. Biomed Rep 2013, 1: 47–52.PubMedPubMed CentralGoogle Scholar
  18. Lobert S, Frankfurter A, Correia JJ: Energetics of vinca alkaloid interactions with tubulin isotypes: implications for drug efficacy and toxicity. Cell Motil Cytoskeleton 1998, 39: 107–121.PubMedView ArticleGoogle Scholar
  19. Sliwkowski MX, Mellman I: Antibody therapeutics in cancer. Science 2013, 341: 192–198.View ArticleGoogle Scholar
  20. Kobayashi Y: Molecular target therapy in hematological malignancy: front-runners and prototypes of small molecule and antibody therapy. Jpn J Clin Oncol 2011, 41: 157–164.PubMedView ArticleGoogle Scholar
  21. Saha MN, Qiu L, Chang H: Targeting p53 by small molecules in hematological malignancies. J Hematol Oncol 2013, 6: 23.PubMedPubMed CentralView ArticleGoogle Scholar
  22. Burnett JC, Rossi JJ, Tiemann K: Current progress of siRNA/shRNA therapeutics in clinical trials. Biotechnol J 2011, 6: 1130–1146.PubMedPubMed CentralView ArticleGoogle Scholar
  23. Kwong-Lam F, Chi-Fung CG: Vincristine could partly suppress stromal support to T-ALL blasts during pegylated arginase I treatment. Exp Hematol Oncol 2013, 2: 11.PubMedPubMed CentralView ArticleGoogle Scholar
  24. Huang B, Zhou H, Wang X, Liu Z: Silencing SATB1 with siRNA inhibits the proliferation and invasion of small cell lung cancer cells. Cancer Cell Int 2013, 13: 8.PubMedPubMed CentralView ArticleGoogle Scholar
  25. Brien G, Trescol-Biemont MC, Bonnefoy-Bérard N: Downregulation of Bfl-1 protein expression sensitizes malignant B cells to apoptosis. Oncogene 2007, 26: 5828–5832.PubMedView ArticleGoogle Scholar
  26. Kang MH, Kang YH, Szymanska B, Wilczynska-Kalak U, Sheard MA, Harned TM, Lock RB, Reynolds CP: Activity of vincristine, L-ASP, and dexamethasone against acute lymphoblastic leukemia is enhanced by the BH3-mimetic ABT-737 in vitro and in vivo. Blood 2007, 110: 2057–2066.PubMedView ArticleGoogle Scholar
  27. High LM, Szymanska B, Wilczynska-Kalak U, Barber N, O'Brien R, Khaw SL, Vikstrom IB, Roberts AW, Lock RB: The Bcl-2 homology domain 3 mimetic ABT-737 targets the apoptotic machinery in acute lymphoblastic leukemia resulting in synergistic in vitro and in vivo interactions with established drugs. Mol Pharmacol 2010, 77: 483–494.PubMedView ArticleGoogle Scholar
  28. George J, Banik NL, Ray SK: Combination of taxol and Bcl-2 siRNA induces poptosis in human glioblastoma cells and inhibits invasion, angiogenesis and tumour growth. J Cell Mol Med 2009, 13: 4205–4218.PubMedPubMed CentralView ArticleGoogle Scholar
  29. Nagamatsu K, Tsuchiya F, Oguma K, Maruyama H, Kano R, Hasegawa A: The effect of small interfering RNA (siRNA) against the Bcl-2 gene on apoptosis and chemosensitivity in a canine mammary gland tumor cell line. Res Vet Sci 2008, 84: 49–55.PubMedView ArticleGoogle Scholar
  30. He D, Fang B: Small hairpin RNA targeting at Bcl-2 increases cytarabine-induced apoptosis in Raji cells. Acta Biochim Biophys Sin 2009, 41: 131–136.PubMedView ArticleGoogle Scholar
  31. Gu L, Zhu N, Zhang H, Durden DL, Feng Y, Zhou M: Regulation of XIAP translation and induction by MDM2 following irradiation. Cancer Cell 2009, 15: 363–375.PubMedPubMed CentralView ArticleGoogle Scholar
  32. Barbieri E, Mehta P, Chen Z, Zhang L, Slack A, Berg S, Shohet JM: MDM2 inhibition sensitizes neuroblastoma to chemotherapy-induced apoptotic cell death. Mol Cancer Ther 2006, 5: 2358–2365.PubMedView ArticleGoogle Scholar
  33. Michaelis M, Rothweiler F, Klassert D, von Deimling A, Weber K, Fehse B, Kammerer B, Doerr HW, Cinatl J Jr: Reversal of P-glycoprotein-mediated multidrug resistance by the murine double minute 2 antagonist nutlin-3. Cancer Res 2009, 69: 416–421.PubMedView ArticleGoogle Scholar
  34. Fan M, Goodwin ME, Birrer MJ, Chambers TC: The c-Jun NH(2)-terminal protein inase/AP-1 pathway is required for efficient apoptosis induced by vinblastine. Cancer Res 2001, 61: 4450–4458.PubMedGoogle Scholar
  35. Groninger E, Meeuwsen-De Boer GJ, De Graaf SS, Kamps WA, De Bont ES: Vincristine induced apoptosis in acute lymphoblastic leukaemia cells: a mitochondrial controlled pathway regulated by reactive oxygen species? Int J Oncol 2002, 21: 1339–1345.PubMedGoogle Scholar

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© He et al.; licensee BioMed Central Ltd. 2014

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