期刊论文详细信息
BMC Cancer
Bax expression measured by AQUAnalysis is an independent prognostic marker in oral squamous cell carcinoma
Pinaki Bose4  Alexander C Klimowicz4  Elizabeth Kornaga4  Stephanie K Petrillo4  T Wayne Matthews3  Shamir Chandarana3  Anthony M Magliocco1  Nigel T Brockton2  Joseph C Dort3 
[1] Present Address: H. Lee Moffitt Cancer Center & Research Institute, 12902 Magnolia Drive, Tampa, FL, 33612, USA
[2] Department of Population Health Research, Alberta Health Services – Cancer Care, Calgary, Canada
[3] Division of Otolaryngology-Head and Neck Surgery, University of Calgary, Calgary, Canada
[4] Department of Oncology, University of Calgary, Calgary, Canada
关键词: prognosis;    Oral cancer;    Bcl-XL;    Bcl-2;    Bax;    AQUA;   
Others  :  1080276
DOI  :  10.1186/1471-2407-12-332
 received in 2012-04-25, accepted in 2012-07-27,  发布年份 2012
PDF
【 摘 要 】

Background

Resistance to apoptosis is a hallmark of cancer and proteins regulating apoptosis have been proposed as prognostic markers in several malignancies. However, the prognostic impact of apoptotic markers has not been consistently demonstrated in oral squamous cell carcinoma (OSCC). This inconsistency in reported associations between apoptotic proteins and prognosis can be partly attributed to the intrinsic low resolution and misclassification associated with manual, semi-quantitative methods of biomarker expression measurement. The aim of this study was to examine the association between apoptosis-regulating proteins and clinical outcomes in oral squamous cell carcinoma (OSCC) using the quantitative fluorescence immunohistochemistry (IHC) based AQUAnalysis technique.

Methods

Sixty-nine OSCC patients diagnosed between 1998–2005 in Calgary, Alberta, Canada were included in the study. Clinical data were obtained from the Alberta Cancer Registry and chart review. Tissue microarrays (TMAs) were assembled from triplicate cores of formalin-fixed paraffin embedded pre-treatment tumour tissue. Bax, Bcl-2 and Bcl-XL protein expression was quantified using fluorescent IHC and AQUA technology in normal oral cavity squamous epithelium (OCSE) and OSCC tumour samples. Survival was analyzed using Kaplan-Meier plots and the Cox proportional hazard model.

Results

Bax expression was predominantly nuclear in OCSE and almost exclusively cytoplasmic in OSCC. No similar differences in localization were observed for Bcl-2 or Bcl-XL. Only Bax expression associated with disease-specific survival (DSS), with 5-year survival estimates of 85.7% for high Bax versus 50.3% for low Bax (p = 0.006), in univariate analysis. High Bax expression was also significantly associated with elevated Ki67 expression, indicating that increased proliferation might lead to an improved response to radiotherapy in patients with elevated Bax expression. In multivariate analyses, Bax protein expression remained an independent predictor of DSS in OSCC [HR 0.241 (0.078-0.745), p = 0.013].

Conclusions

The AQUA technique used in our study eliminates observer bias and provides reliable and reproducible estimates for biomarker expression. AQUA also provides essential measures of quality control that cannot be achieved with manual biomarker scoring techniques. Our results support the use of Bax protein expression as a prognostic marker in conjunction with other clinico-pathological variables when designing personalized treatment strategies for OSCC patients.

【 授权许可】

   
2012 Bose et al.; licensee BioMed Central Ltd.

【 预 览 】
附件列表
Files Size Format View
20141202235116125.pdf 2354KB PDF download
Figure 5. 48KB Image download
Figure 4. 129KB Image download
Figure 1. 19KB Image download
Figure 2. 135KB Image download
Figure 1. 62KB Image download
【 图 表 】

Figure 1.

Figure 2.

Figure 1.

Figure 4.

Figure 5.

【 参考文献 】
  • [1]Parkin DM, Bray F, Ferlay J, Pisani P: Global cancer statistics, 2002. CA Cancer J Clin 2005, 55:74-108.
  • [2]Campana JP, Meyers AD: The surgical management of oral cancer. Otolaryngol Clin North Am 2006, 39:331-348.
  • [3]Massano J, Regateiro FS, Januario G, Ferreira A: Oral squamous cell carcinoma: review of prognostic and predictive factors. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2006, 102:67-76.
  • [4]Oliveira LR, Ribeiro-Silva A: Prognostic significance of immunohistochemical biomarkers in oral squamous cell carcinoma. Int J Oral Maxillofac Surg 2011, 40:298-307.
  • [5]Haraf DJ, Nodzenski E, Brachman D, Mick R, Montag A, Graves D, Vokes EE, Weichselbaum RR: Human papilloma virus and p53 in head and neck cancer: clinical correlates and survival. Clin Cancer Res 1996, 2:755-762.
  • [6]Syrjanen S, Shabalova I, Petrovichev N, Kozachenko V, Zakharova T, Pajanidi J, Podistov J, Chemeris G, Sozaeva L, Lipova E, et al.: Acquisition of high-risk human papillomavirus infections and pap smear abnormalities among women in the New Independent States of the Former Soviet Union. J Clin Microbiol 2004, 42:505-511.
  • [7]Ragin CC, Taioli E: Survival of squamous cell carcinoma of the head and neck in relation to human papillomavirus infection: review and meta-analysis. Int J Cancer 2007, 121:1813-1820.
  • [8]Lopes V, Murray P, Williams H, Woodman C, Watkinson J, Robinson M: Squamous cell carcinoma of the oral cavity rarely harbours oncogenic human papillomavirus. Oral Oncol 2011, 47:698-701.
  • [9]Hanahan D, Weinberg RA: The hallmarks of cancer. Cell 2000, 100:57-70.
  • [10]Hanahan D, Weinberg RA: Hallmarks of cancer: the next generation. Cell 2011, 144:646-674.
  • [11]Kerr JF, Winterford CM, Harmon BV: Apoptosis. Its significance in cancer and cancer therapy. Cancer 1994, 73:2013-2026.
  • [12]Singh BB, Chandler FW: Whitaker SB, Forbes-Nelson AE: Immunohistochemical evaluation of bcl-2 oncoprotein in oral dysplasia and carcinoma. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 1998, 85:692-698.
  • [13]Schoelch ML, Le QT, Silverman S: McMillan A, Dekker NP, Fu KK, Ziober BL, Regezi JA: Apoptosis-associated proteins and the development of oral squamous cell carcinoma. Oral Oncol 1999, 35:77-85.
  • [14]Xie X, Clausen OP, De Angelis P, Boysen M: The prognostic value of spontaneous apoptosis, Bax, Bcl-2, and p53 in oral squamous cell carcinoma of the tongue. Cancer 1999, 86:913-920.
  • [15]Loro LL, Vintermyr OK, Johannessen AC: Cell death regulation in oral squamous cell carcinoma: methodological considerations and clinical significance. J Oral Pathol Med 2003, 32:125-138.
  • [16]Green DR, Evan GI: A matter of life and death. Cancer Cell 2002, 1:19-30.
  • [17]Youle RJ, Strasser A: The BCL-2 protein family: opposing activities that mediate cell death. Nat Rev Mol Cell Biol 2008, 9:47-59.
  • [18]Llambi F, Green DR: Apoptosis and oncogenesis: give and take in the BCL-2 family. Curr Opin Genet Dev 2011, 21:12-20.
  • [19]Oltvai ZN, Milliman CL, Korsmeyer SJ: Bcl-2 heterodimerizes in vivo with a conserved homolog, Bax, that accelerates programmed cell death. Cell 1993, 74:609-619.
  • [20]Korsmeyer SJ, Wei MC, Saito M, Weiler S, Oh KJ, Schlesinger PH: Pro-apoptotic cascade activates BID, which oligomerizes BAK or BAX into pores that result in the release of cytochrome c. Cell Death Differ 2000, 7:1166-1173.
  • [21]Boise LH, Gonzalez-Garcia M, Postema CE, Ding L, Lindsten T, Turka LA, Mao X, Nunez G, Thompson CB: Bcl-x, a bcl-2-related gene that functions as a dominant regulator of apoptotic cell death. Cell 1993, 74:597-608.
  • [22]Camisasca DR, Honorato J, Bernardo V, da Silva LE, da Fonseca EC, de Faria PA, Dias FL, Lourenco SQ: Expression of Bcl-2 family proteins and associated clinicopathologic factors predict survival outcome in patients with oral squamous cell carcinoma. Oral Oncol 2009, 45:225-233.
  • [23]Yuen AP, Lam KY, Choy JT, Ho WK, Wong LY, Wei WI: Clinicopathologic significance of bcl-2 expression in the surgical treatment of oral tongue carcinoma. Eur J Surg Oncol 2002, 28:667-672.
  • [24]de Vicente JC, Olay S, Lequerica-Fernandez P, Sanchez-Mayoral J, Junquera LM, Fresno MF: Expression of Bcl-2 but not Bax has a prognostic significance in tongue carcinoma. J Oral Pathol Med 2006, 35:140-145.
  • [25]Kato K, Kawashiri S, Yoshizawa K, Kitahara H, Yamamoto E: Apoptosis-associated markers and clinical outcome in human oral squamous cell carcinomas. J Oral Pathol Med 2008, 37:364-371.
  • [26]Zhang M, Zhang P, Zhang C, Sun J, Wang L, Li J, Tian Z, Chen W: Prognostic significance of Bcl-2 and Bax protein expression in the patients with oral squamous cell carcinoma. J Oral Pathol Med 2009, 38:307-313.
  • [27]Camp RL, Chung GG, Rimm DL: Automated subcellular localization and quantification of protein expression in tissue microarrays. Nat Med 2002, 8:1323-1327.
  • [28]McShane LM, Altman DG, Sauerbrei W, Taube SE, Gion M, Clark GM: REporting recommendations for tumour MARKer prognostic studies (REMARK). Eur J Cancer 2005, 41:1690-1696.
  • [29]Staibano S, Mignogna MD, Lo Muzio L, Di Alberti L, Di Natale E, Lucariello A, Mezza E, Bucci E, DeRosa G: Overexpression of cyclin-D1, bcl-2, and bax proteins, proliferating cell nuclear antigen (PCNA), and DNA-ploidy in squamous cell carcinoma of the oral cavity. Hum Pathol 1998, 29:1189-1194.
  • [30]Coutinho-Camillo CM, Lourenco SV, Nishimoto IN, Kowalski LP, Soares FA: Expression of Bcl-2 family proteins and association with clinicopathological characteristics of oral squamous cell carcinoma. Histopathology 2010, 57:304-316.
  • [31]Giannopoulou I, Nakopoulou L, Zervas A, Lazaris AC, Stravodimos C, Giannopoulos A, Davaris PS: Immunohistochemical study of pro-apoptotic factors Bax, Fas and CPP32 in urinary bladder cancer: prognostic implications. Urol Res 2002, 30:342-345.
  • [32]Schelwies K, Sturm I, Grabowski P, Scherubl H, Schindler I, Hermann S, Stein H, Buhr HJ, Riecken EO, Zeitz M, et al.: Analysis of p53/BAX in primary colorectal carcinoma: low BAX protein expression is a negative prognostic factor in UICC stage III tumors. Int J Cancer 2002, 99:589-596.
  • [33]Kang SY, Oh YT, Han JH, Choi JH, Lim HY, Kim HI, Lee HW, Jang JH, Park JS, Kim HC, et al.: Concurrent chemoradiotherapy in patients with nasopharyngeal cancer: prognostic significance of low expression of bax. Neoplasma 2006, 53:450-456.
  • [34]Agrawal SG, Liu FT, Wiseman C, Shirali S, Liu H, Lillington D, Du MQ, Syndercombe-Court D, Newland AC, Gribben JG, et al.: Increased proteasomal degradation of Bax is a common feature of poor prognosis chronic lymphocytic leukemia. Blood 2008, 111:2790-2796.
  • [35]Jeong SH, Han JH, Kim JH, Ahn MS, Hwang YH, Lee HW, Kang SY, Park JS, Choi JH, Lee KJ, et al.: Bax predicts outcome in gastric cancer patients treated with 5-fluorouracil, leucovorin, and oxaliplatin palliative chemotherapy. Dig Dis Sci 2011, 56:131-138.
  • [36]Zhan Q, Fan S, Bae I, Guillouf C, Liebermann DA, O'Connor PM, Fornace AJ: Induction of bax by genotoxic stress in human cells correlates with normal p53 status and apoptosis. Oncogene 1994, 9:3743-3751.
  • [37]Bai M, Skyrlas A, Agnantis NJ, Kamina S, Kitsoulis P, Kanavaros P: Cluster analysis of apoptosis-associated bcl2 family proteins in diffuse large B-cell lymphomas. Relations with the apoptotic index, the proliferation profile and the B-cell differentiation immunophenotypes. Anticancer Res 2004, 24:3081-3088.
  • [38]Kikuchi M, Mikami T, Sato T, Tokuyama W, Araki K, Watanabe M, Saigenji K, Okayasu I: High Ki67, Bax, and thymidylate synthase expression well correlates with response to chemoradiation therapy in locally advanced rectal cancers: proposal of a logistic model for prediction. Br J Cancer 2009, 101:116-123.
  • [39]Brady HJ, Gil-Gomez G, Kirberg J, Berns AJ: Bax alpha perturbs T cell development and affects cell cycle entry of T cells. EMBO J 1996, 15:6991-7001.
  • [40]O'Reilly LA, Huang DC, Strasser A: The cell death inhibitor Bcl-2 and its homologues influence control of cell cycle entry. EMBO J 1996, 15:6979-6990.
  • [41]Verheij M: Clinical biomarkers and imaging for radiotherapy-induced cell death. Cancer Metastasis Rev 2008, 27:471-480.
  • [42]Hoetelmans R, van Slooten HJ, Keijzer R, Erkeland S, van de Velde CJ, Dierendonck JH: Bcl-2 and Bax proteins are present in interphase nuclei of mammalian cells. Cell Death Differ 2000, 7:384-392.
  • [43]Nishita M, Inoue S, Tsuda M, Tateda C, Miyashita T: Nuclear translocation and increased expression of Bax and disturbance in cell cycle progression without prominent apoptosis induced by hyperthermia. Exp Cell Res 1998, 244:357-366.
  • [44]Wang ZH, Ding MX, Chew-Cheng SB, Yun JP, Chew EC: Bcl-2 and Bax proteins are nuclear matrix associated proteins. Anticancer Res 1999, 19:5445-5449.
  • [45]Ma BB, Bristow RG, Kim J, Siu LL: Combined-modality treatment of solid tumors using radiotherapy and molecular targeted agents. J Clin Oncol 2003, 21:2760-2776.
  文献评价指标  
  下载次数:41次 浏览次数:33次