bcl-2 expression is not associated with survival in metastatic cutaneous melanoma: A historical cohort study
© Espíndola and Corleta; licensee BioMed Central Ltd. 2008
Received: 10 December 2007
Accepted: 20 June 2008
Published: 20 June 2008
Programmed cell death (apoptosis) has been implicated in tumor development and may affect the metastatic potential of tumor cells. The role of bcl-2, a proto-oncogene that inhibits apoptosis, has been studied in several malignancies, including cutaneous melanoma (CM). The purpose of this study was to evaluate the immunohistochemical expression of bcl-2 in 35 regional lymph node, 28 subcutaneous and 17 visceral CM metastases, correlating the findings with patient survival.
In a historical cohort study patient survival was correlated with the expression of bcl-2 in regional lymph node, subcutaneous and visceral metastases of CM. Eighty slides containing surgical specimens from 50 patients diagnosed with stage III and IV CM, 28 male (56%) and 22 female (44%), were analyzed. Mean age at diagnosis was 43 years (16–74 years; median = 42 years). Mean Breslow depth was 5.01 mm (0.4–27.5 mm). The slides were submitted to immunohistochemical reaction using anti-bcl-2 monoclonal antibody and classified according to the degree of staining (< 5%; 5 to 50%; or > 50% of tumor cells stained). The relationship between bcl-2 protein expression and survival for each type of metastasis, gender and age at initial diagnosis was analyzed.
Mean overall survival was 33.9 months after the diagnosis of the initial metastatic lesion (range: 0 to 131 months). Twenty-four out of 50 patients (48%) had died from CM by the end of the study period. bcl-2 expression was detected in 74.3, 85.7 and 82.4% of lymph node, subcutaneous and visceral metastases, respectively. After univariate and multivariate analyses, no correlation was found between positive bcl-2 expression and overall survival for the types of metastases evaluated.
The immunohistochemical expression of bcl-2 in metastasis alone is not a prognostic marker for CM.
The incidence of cutaneous melanoma (CM) has increased steadily in the last few years . Sun exposure and sunburn, with subsequent genetic damage caused by ultraviolet radiation , play a major role in this increase. The prognosis of CM is positive in its initial stages; however, the five-year survival rate is only 41% in patients with regional lymph node metastases. A maximum survival of 2 years has been reported for patients with distant metastases .
Despite major advances in cancer treatment, surgery is still the treatment of choice for CM, since chemotherapy and radiation therapy generally produce low response rates [4, 5]. Since the ultimate goal of non-surgical treatments is to induce apoptosis in tumor cells, this physiological event has recently received much attention . Defects in the regulation of apoptosis have been implicated in tumor progression, metastatic spread and resistance to chemotherapy [7, 8]. In recent years, several biomolecules, including B cell lymphoma/leukemia-2 (bcl-2), have been studied in CM, in an attempt to determine which lesions are more likely to respond to non-surgical treatments .
The bcl-2 gene is located on chromosome segment 18q21.3, in a telomere-centromere orientation . The bcl-2 protein is an integral part of the cell membrane, with a molecular weight of 26 kDa, and it is found in the cell nucleus, mitochondria and endoplasmic reticulum . bcl-2 acts as an apoptosis inhibitor, without any influence on cell proliferation .
The results obtained so far for the role of bcl-2 in CM are controversial. Although some authors have described an increase in bcl-2 during the progression of normal melanocytes to melanomas, others have observed the opposite [11–15]. Grover et al.  have reported a lower survival rate in CM patients with regional lymph node metastasis and positive bcl-2 expression.
The purpose of the present study was to evaluate the relationship between the immunohistochemical expression of bcl-2 and survival in patients with regional lymph node, subcutaneous and visceral metastases of CM.
Patients and methods
In this historical cohort study, the survival of patients with CM represents the outcome, and the expression of bcl-2 in regional lymph node, subcutaneous and visceral metastases of CM is the variable of interest.
Eighty slides containing surgical specimens from 50 patients treated at three institutions between 1990 and 2007, 28 male (56%) and 22 female (44%), were analyzed. All patients had been diagnosed with stage III (regional metastases) and stage IV (distant metastases) CM . In all cases, initial resection was performed at one of the participating hospitals. Exclusion criteria were previous diagnosis of other types of cancer, simultaneous diagnosis of secondary neoplasm, previous radiation therapy, chemotherapy or resection of metastases prior to diagnosis, initial surgery for metastasis at a different institution, incomplete resection of metastases, or death due to causes other than CM. The study was approved by the Hospital de Clínica de Porto Alegre Research Ethics Committee (IRB equivalent).
Distribution of 50 patients with cutaneous melanoma in terms of primary diagnosis and location of tumor and first metastasis
Primary tumor diagnosis
Superficial spreading CM
Head and neck
Site of first metastasis
If more than one metastasis was present in the same site, only the first metastasis at each site was evaluated for bcl-2 protein expression. Thirty patients did not receive any treatments other than surgery. Of the remaining 20 patients, nine received chemotherapy, with regimens that included the following drugs: dacarbazine (DTIC), carmustine (BCNU), verapamil, cisplatin and tamoxifen, in varying combinations and for one to five treatment cycles. One patient received hyperthermic isolated lower limb perfusion with melphalan; complete response was observed immediately after treatment, but a relapse occurred later. Five patients were treated with interferon for 1 to 5 months. Five patients received radiation therapy, of whom four were treated for central nervous system (CNS) metastases and one for disease in the axilla, all with palliative intent.
Sections of paraffin-embedded metastasis specimens were initially stained with hematoxylin-eosin for evaluation of tumor representation. The chosen blocks were sliced into 4-μm sections and stored in an incubator at 56°C for 24 h. After deparaffinization and hydration by immersion in xylol and decreasing concentrations of ethanol (100 to 20%) in room temperature, antigenic recovery was carried out using the microwave irradiation method. After that, the specimens were rinsed in tap water and distilled water and immersed in PBS buffer for 5 min. To block tissue enzymes that could interfere with the reaction, the endogenous peroxidase method was employed. To block unspecific reactions that could yield false-positive results, powder milk was used, with rehydration in 5% PBS buffer for 40 min, washing in tap water and distilled water and immersion in PBS for 5 min. The specific antibody reaction was carried out with bcl-2 antibody (IgG 1, kappa, 280 mg/L – Monoclonal Mouse Anti-Human bcl-2 Oncoprotein Clone 124 Code no. M0887 Lot 018; Dako Corporation, Carpinteria, CA, USA) diluted in PBS buffer (1:500). The sections were then stored in a dark chamber for 1 hour at 37°C or left at 4°C in a refrigerator overnight. The slides were individually washed three times for 5 min in PBS buffer. Secondary antibody (DAKO/LSAB – Dako Liquid DAB Large Volume Substrate-Chromogen System Code N°: K3466; Dako Corporation, Carpinteria, CA, USA) was applied for 30 minutes, followed by three 5-min baths with PBS buffer. The DAB kit was used for development. Counterstaining was carried out with Harris hematoxylin for 20 s after serial rinsing with tap water, 2% ammonia solution, ethanol and xylol.
0 (negative): less than 5% of tumor cells stained with bcl-2;
I (weakly positive): 5 to 50% of tumor cells stained with bcl-2;
II (strongly positive): over 50% of tumor cells stained with bcl-2.
Since statistical analysis did not reveal differences between groups I and II, they were considered as one group (bcl-2-positive) for the present analysis. Results are presented as arithmetic means, standard deviation, medians, and percentage rates. The chi-square test, Fisher's exact test, log-rank test, and Kaplan Meier method were used to evaluate the relationship between bcl-2 protein expression and survival for the three types of metastases (regional lymph node, subcutaneous and visceral metastases), gender and age at initial diagnosis, with 95% confidence intervals. Univariate and multivariate Cox regression tests were performed to evaluate the interaction between gender, age at first metastasis, survival, type of metastasis, and bcl-2 expression. A P < 0.05 was considered to be statistically significant.
Mean overall survival was 33.9 months after the diagnosis of the initial metastatic lesion (range: 0 to 131 months). Twenty-four out of 50 patients (48%) had died from CM by the end of the study period. Of the 26 surviving patients, nine (36%) had imaging exams suggestive of multiple metastatic lesions or a single unresectable metastatic lesion. The mean disease-free interval (from initial diagnosis to the diagnosis of the first metastasis) was 17.6 months (0 to 83 months) (median of 11.5 months and standard deviation of 21.5 months). Five patients (10%) had visceral and subcutaneous metastases simultaneously, and one (2%) had the three types of metastasis since the start of metastatic disease.
Immunohistochemical expression of bcl-2 and deaths in patients with cutaneous melanoma
Lymph node metastases
(n = 35)
(n = 28)
(n = 17)
Chi-square test results for expression of bcl-2 in three types of metastases
bcl-2 positive (%)
bcl-2 negative (%)
Survival was correlated with age > 60 years at initial diagnosis (log rank = 6.17; P = 0.130) and male gender (log rank = 3.17; P = 0.0752) in patients with subcutaneous metastases. None of the other comparisons between survival, age, gender, and bcl-2 expression were statistically significant. Similar results were obtained using univariate analysis (P > 0.05) and Cox's multivariate analysis.
Apoptosis, or programmed cell death, has recently become the focus of great interest [7, 9, 17]. Discovery of the bcl-2 gene, an apoptosis inhibitor, in translocation 14;18 (q32;q21) in follicular B-cell lymphomas, followed by the identification of the BCL-2 family in the study of Caenorhabditis elegans, opened new perspectives for the study of tissue morphogenesis and oncogenesis [9, 11, 18].
Inhibition of apoptosis can occur in any phase of the cell cycle, although the exact mechanism through which bcl-2 inhibits apoptosis is not fully understood . In the presence of bcl-2 overexpression, the ability of the cell to remove genetic and cell damage through apoptosis is limited. Despite the fact that bcl-2 does not act directly on cell proliferation, its overexpression enables tumors to progress to highly malignant phenotypes and to become more resistant to chemotherapy and apoptosis-inducing radiation therapy, with subsequent metastatic spread and tumor progression [8, 19, 20].
Several different tissues express the bcl-2 protein. In some types of neoplasms originating from these tissues (such as lymph nodes with breast cancer metastasis), a relationship between bcl-2 expression and longer disease-free survival has been observed. On the other hand, in other tumor types, there is an inverse relationship between positive bcl-2 expression and prognosis, such as in prostate cancer, ovarian cancer, non-small cell lung cancer, follicular thyroid cancer, neuroblastoma, and breast cancer [14, 15]. In the case of CM, this relationship is still controversial and undefined.
Confounding variables such as sample size, gender and age should be considered when studying prognostic factors in CM. The relatively small number of cases analyzed in our study is due mainly to the absence of appropriate protocols for the management of CM in our setting, making it more difficult to gather patient information. Moreover, it is often not possible to retrieve data from inaccurate patient charts, and pathology divisions, at least in our institutions, lack an appropriate database, which would facilitate the access to patient charts using pathology diagnosis as a search variable.
The ages of 50 and 60 years have been used as cutoff points for the evaluation of CM patients [3, 21–23]. In this study, we observed that patients older than 60 years were at greater risk for subcutaneous metastases of CM, and also that age had no effect on the survival of patients with other types of metastasis. The larger tumor thickness found in patients older than 60 years at diagnosis, as well as the accumulation of genetic damage acquired throughout the years, may account for these findings . Fernandez-Pol and Douglas related the presence of bcl-2, mitochondrial integrity and carcinogenesis with human aging . Garbe and Blum noticed that most melanomas were diagnosed between the sixth and seventh decades of life, with only 22% of the cases diagnosed before the age of 40 .
We were unable to evaluate the histological characteristics of primary tumors because this information was not available for all cases. Also, we did not analyze the relationship between location of the primary lesion, survival and bcl-2. Nevertheless, the characteristics of the primary lesion lose some importance once the first metastasis is diagnosed [3, 22, 27–29]. The importance of data about the primary tumor is in fact controversial, with different authors reporting conflicting results about the role of pathology data and primary site location in CM prognosis [1, 3, 21, 23, 27, 30, 31].
In addition, the expression of bcl-2 in CM metastases was evaluated without comparison to bcl-2 expression in normal melanocytes. That comparison was not performed because this is a retrospective study, based on paraffin block specimens and on medical records. It was therefore not possible to obtain normal skin or nevus samples from the patients enrolled in the study. Nevertheless, bcl-2 expression in our study was similar to that described in previous studies employing immunohistochemical methods [14, 15, 32, 33].
We did not observe a relationship between bcl-2 expression and survival in the three types of CM metastasis. This could be explained in three distinct ways: first, there is no correlation between survival and the immunohistochemical expression of bcl-2 in CM; second, this correlation exists, but was not demonstrated in the present study due to the small sample size and short follow-up time; and third, the interaction between the other members of the BCL-2 family may have neutralized the expression of bcl-2. The regulation of proapoptotic and antiapoptotic components in the BCL-2 family is complex. Several members of this family are still being discovered, such as Bim and GRS [34, 35], and the complex interactions between BCL-2 family members are only partially understood. In the future, a deeper understanding of these interactions, and mainly of their functions (rather than only of their presence), may allow for an adequate use of BCL-2 family members as effective predictors of survival in CM.
It has been shown that the treatment of melanoma cells with oligonucleotides targeting the reduction of bcl-2 expression rendered those cells more sensitive to chemotherapy [5, 36–41]. These oligonucleotides are chemically modified, single-stranded DNA that complement specific codons of the messenger-RNA of a target gene, and which are capable of inhibiting the expression of this particular gene . These experiments demonstrate that bcl-2 protein plays an important, although not fully understood, role in chemoresistance in CM and several other tumors [37, 38].
The present results suggest that the immunohistochemical expression of bcl-2 in metastases alone is not a prognostic marker for CM. Further knowledge of the actions and relations between BCL-2 family members is necessary to define the exact role of the bcl-2 protein and of other BCL-2 family members in the pathogenesis, prognosis, and response of metastatic CM to new treatments.
The authors wish to thank Dr. Luis Fernando Rivero, Professor of Pathology of at Universidade Federal do Rio Grande do Sul (UFRGS), for his support and guidance in the interpretation of immunohistochemical data.
The study was approved by the ethics committee.
- Markowitz JS, Cosimi LA, Carey RW, Kang S, Padyk C, Sober AJ, Cosimi AB: Prognosis after initial recurrence of cutaneous melanoma. Arch Surg. 1991, 126: 703-708.View ArticlePubMedGoogle Scholar
- Gilchrest BA, Eller MS, Geller AC, Yaar M: The pathogenesis of melanoma induced by ultraviolet radiation. NEJM. 1999, 340: 1341-1348. 10.1056/NEJM199904293401707.View ArticlePubMedGoogle Scholar
- Stadelmann WK, Rapaport DP, Soong S-J, Reintgen DS, Buzaid AC, Balch CM: Prognostic Clinical pathologic features. Cutaneous melanoma. Edited by: Balch CM, Houghton AN, Sober AJ, Soong S-J. 1998, St. Louis, Missouri: Quality Medical Publishing, Inc, 11-35. 3Google Scholar
- Rünger TM, Emmert S, Schadendorf D, Diem C, Epe B, Hllfritsch D: Alterations of repair in melanoma cell lines resistant to Cisplatin, Fotemustine, or Etoposide. J Invest Dermatol. 2000, 114: 34-39. 10.1046/j.1523-1747.2000.00844.x.View ArticlePubMedGoogle Scholar
- Jansen B, Schlagbauer-Wadl H, Brown BD, Bryan RN, van Elsas A, Müller M, Wollf K, Eichler HG, Pehamberger H: bcl-2 antisense therapy chemosensitizes human melanoma in SCDI mice. Nat Med. 1998, 4: 232-234. 10.1038/nm0298-232.View ArticlePubMedGoogle Scholar
- Miller LJ, Marx J: Apoptosis [editorial]. Science. 1998, 281: 1301-10.1126/science.281.5381.1301.View ArticleGoogle Scholar
- Meterissian SH: Apoptosis: its role in the progression of and chemotherapy for carcinoma. J Am Col Surg. 1997, 184: 658-666.Google Scholar
- Wong CW, Lee A, Shientag L, Yu J, Dong Y, Kao G, Al-Mehdi AB, Bernhard EJ, Mushel RJ: Apoptosis: an early event in metastatic inefficiency. Cancer Res. 2001, 61: 333-338.PubMedGoogle Scholar
- Korsmeyer SJ: Bcl-2 initiates a new category of oncogenes: regulators of cell death. Blood. 1992, 80: 879-886.PubMedGoogle Scholar
- Reed JA, Albino AP: Update of diagnostic and prognostic markers in cutaneous malignant melanoma. Dermatol Clin. 1999, 17: 631-643. 10.1016/S0733-8635(05)70112-1.View ArticlePubMedGoogle Scholar
- Grover R, Wilson GD: Bcl-2 expression in malignant melanoma and its prognostic significance. Eur J Surg Oncol. 1996, 22: 347-349. 10.1016/S0748-7983(96)90176-6.View ArticlePubMedGoogle Scholar
- Mikhail M, Velasquez E, Shapiro R, Berman R, Pavlik A, Sorhaindo L, Spira J, Mir C, Panageas KS, Polsky D, Osman I: PTEN expression in melanoma: relationship with patient survival, Bcl-2 expression, and proliferation. Clin Cancer Res. 2005, 11: 5153-5157. 10.1158/1078-0432.CCR-05-0397.View ArticlePubMedGoogle Scholar
- Tron VA, Krajewski S, Klein-Parker H, Li G, Ho VC, Reed JC: Immunohistochemical analysis of bcl-2 protein regulation in cutaneous melanoma. Am J Pathol. 1995, 146: 643-650.PubMed CentralPubMedGoogle Scholar
- Tang L, Tron VA, Reed JC, Mah KJ, Krajewska M, Li G, Zhou X, Ho VC, Trotter MJ: Expression of apoptosis regulators in cutaneous malignant melanoma. Clin Cancer Res. 1998, 4: 1865-1871.PubMedGoogle Scholar
- Leiter U, Schmid RL, Kaskel P, Peter RA, Krähn G: Antiapoptotic bcl-2 and bclxL in advanced melanoma. Arch Dermatol Res. 2000, 292: 225-232. 10.1007/s004030050479.View ArticlePubMedGoogle Scholar
- Balch CB, Buzaid AC, Atking MB, Cascinelli N, Coit DG, Fleming ID, Houghton A, Kirkwood JM, Mihm MF, Morton DL, Reintgen D, Ross MI, Sober A, Soong S-J, Thompson JA, Thompson JF, Gershenwald JE, McMasters KM, for the AJCC Melanoma Staging Committee: A New American Joint Committee on Cancer staging system for cutaneous melanoma. Cancer. 2000, 88: 1484-1491. 10.1002/(SICI)1097-0142(20000315)88:6<1484::AID-CNCR29>3.0.CO;2-D.View ArticlePubMedGoogle Scholar
- Carson DA, Ribeiro JM: Apoptosis and disease. Lancet. 1993, 341: 1251-1254. 10.1016/0140-6736(93)91154-E.View ArticlePubMedGoogle Scholar
- Plettenberg A, Ballaun C, Pammer J, Mildner M, Strunk D, Weninger W, Tschachler E: Human melanocytes and melanoma cells constitutively express the bcl-2 proto-oncogene in situ and in cell culture. Am J Pathol. 1995, 146: 651-659.PubMed CentralPubMedGoogle Scholar
- Lu Q-L, Abel P, Foster C, Lalani E-N: bcl-2: role in epithelial differentiation and oncogenesis. Hum Pathol. 1996, 27: 102-110. 10.1016/S0046-8177(96)90362-7.View ArticlePubMedGoogle Scholar
- Takaoka A, Adachi M, Okuda H, Sato S, Yawata A, Hinoda Y, Takayama S, Reed JC, Imai K: Anti-cell death activity promotes pulmonary metastasis of melanoma cells. Oncogene. 1997, 14: 2971-2977. 10.1038/sj.onc.1201147.View ArticlePubMedGoogle Scholar
- Drzewiecki KT, Andersen K: Survival with malignant melanoma – A regression analysis of prognostic factors. Cancer. 1982, 49: 2414-2419. 10.1002/1097-0142(19820601)49:11<2414::AID-CNCR2820491132>3.0.CO;2-V.View ArticlePubMedGoogle Scholar
- Gershenwald JE, Sussman JJ, Lee JE: Melanoma. The MD Anderson surgical oncology handbook. Edited by: Feig BW, Berger DH, Fuhrman GM. 1999, Philadelphia: Lippincott Williams and Wilkins, 38-68. 2Google Scholar
- Barth A, Wanek LA, Morton CL: Prognostic factors in 1,521 melanoma patients with distant metastases. J Am Coll Surg. 1995, 181: 193-201.PubMedGoogle Scholar
- Osborne JE, Hutchinson PE: Clinical correlates of Breslow thickness of malignant melanoma. Br J Dermatol. 2001, 144: 476-483. 10.1046/j.1365-2133.2001.04071.x.View ArticlePubMedGoogle Scholar
- Fernandez-Pol JA, Douglas MG: Molecular interactions of cancer and age. Hem/Oncol Clin North Am. 2000, 14: 25-44.View ArticleGoogle Scholar
- Garbe C, Blum A: Epidemiology of cutaneous melanoma in Germany and worldwide [abstract]. Skin Pharmacol Appl Skin Physiol. 2001, 14: 280-290. 10.1159/000056358.View ArticlePubMedGoogle Scholar
- Ryan L, Kramar A, Borden E: Prognostic factors in metastatic melanoma. Cancer. 1993, 71: 2995-3005. 10.1002/1097-0142(19930515)71:10<2995::AID-CNCR2820711018>3.0.CO;2-P.View ArticlePubMedGoogle Scholar
- Eberlein TJ: Prognosis of patients with advanced melanoma. J Am Coll Surg. 1995, 181: 263-265.PubMedGoogle Scholar
- Presant CA, Bartolucci AA, Southeastern Cancer Study Group: Prognostic factors in metastatic malignant melanoma – the southeastern cancer study group experience. Cancer. 1982, 49: 2192-2196. 10.1002/1097-0142(19820515)49:10<2192::AID-CNCR2820491035>3.0.CO;2-R.View ArticlePubMedGoogle Scholar
- Shaw HM, McGovern VJ, Milton GW, Faraco GA, McCarthy WH: Histologic features of tumors and the female superiority in survival from malignant melanoma. Cancer. 1980, 45: 1604-1608. 10.1002/1097-0142(19800401)45:7<1604::AID-CNCR2820450715>3.0.CO;2-O.View ArticlePubMedGoogle Scholar
- Balch CM, Soong SJ, Gershenwald JE, Thompson JF, Reintgen DS, Cascinelli N, Urist M, MacMasters KM, Ross MI, Kirkwood JM, Atkins MB, Thompson JA, Coit DG, Byrd D, Desmond R, Zhang Y, Liu PY, Lyman GH, Morabito A: Prognostic factors analysis of 17,600 melanoma patients: validation of the American Joint Committee on Cancer melanoma staging system. J Clin Oncol. 2001, 19: 3622-3634.PubMedGoogle Scholar
- Collins KA, White WL: Intercellular adhesion molecule 1 (ICAM-1) and bcl-2 are differentially expressed in early evolving malignant melanoma. Am J Dermatopathol. 1995, 17: 429-438.View ArticlePubMedGoogle Scholar
- Morales-Ducret CRJ, Rijn van de M, LeBrun DP, Smoller BR: Bcl-2 expression in primary malignancies of the skin. Arch Dermatol. 1995, 131: 909-912. 10.1001/archderm.131.8.909.View ArticlePubMedGoogle Scholar
- O'Connor L, Strasser A, O'Reilly LA, Hausmann G, Adams JM, Cory S, Huang DC: Bim: a novel member of the bcl-2 family that promotes apoptosis. EMBO J. 1998, 17: 384-395. 10.1093/emboj/17.2.384.PubMed CentralView ArticlePubMedGoogle Scholar
- Kenny JJ, Knobloch TJ, Augustus M, Carter KC, Rosen CA, Lang JC: GRS, a novel member of the bcl-2 gene family, is highly expressed in multiple cancer cell lines and in normal leukocytes. Oncogene. 1997, 14: 997-1001. 10.1038/sj.onc.1200898.View ArticlePubMedGoogle Scholar
- Jansen B, Wacheck V, Heere-ress E, Schlagbauer-Wadl H, Hoeller C, Lucas T, Hoermann M, Hollenstein U, Wolff K, Pehamberger H: Chemosensitisation of malignant melanoma by BCL2 antisense therapy. Lancet. 2000, 356: 1728-1733. 10.1016/S0140-6736(00)03207-4.View ArticlePubMedGoogle Scholar
- Letai A: Pharmacological manipulation of Bcl-2 family members to control cell death. J Clin Invest. 2005, 115: 2648-2655. 10.1172/JCI26250.PubMed CentralView ArticlePubMedGoogle Scholar
- Alvarez MG, Besa PC: Molecular basis of cancer and clinical applications. Surg Clin North America. 2000, 80: 443-457. 10.1016/S0039-6109(05)70194-8.View ArticleGoogle Scholar
- Wolter KG, Verhaegen M, Fernandez Y, Nikolovska-Coleska Z, Riblett M, de la Vega CM, Wang S, Soengas MS: Therapeutic window for melanoma treatment provided by selective effects of the proteasome on Bcl-2 proteins. Cell Death Differ. 2007, 14 (9): 1605-1616. 10.1038/sj.cdd.4402163.View ArticlePubMedGoogle Scholar
- Tarhini AA, Kirkwood JM: Oblimersen in the treatment of metastatic melanoma. Future Oncol. 2007, 3: 263-271. 10.2217/147966188.8.131.523.View ArticlePubMedGoogle Scholar
- Mena S, Benlloch M, Ortega A, Carretero J, Obrador E, Asensi M, Petschen I, Brown BD, Estrela JM: Bcl-2 and glutathione depletion sensitizes B16 melanoma to combination therapy and eliminates metastatic disease. Clin Cancer Res. 2007, 9: 2658-2666. 10.1158/1078-0432.CCR-06-2642.View ArticleGoogle Scholar
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