J Breast Cancer.  2007 Mar;10(1):19-28. 10.4048/jbc.2007.10.1.19.

Prognostic Value of Apoptosis and the Survivin, bcl-2, and p53 Expressions in Breast Cancer Patients

Affiliations
  • 1Department of Surgery, Soonchunhyang University Cheonan Hospital, College of Medicine, Cheonan, Korea. sykim@schch.co.kr
  • 2Department of Surgery, Dangjin Green Hospital, Dangjin, Korea.
  • 3Department of Physiology, Soonchunhyang University Cheonan Hospital, College of Medicine, Cheonan, Korea.
  • 4Department of Pathology, Soonchunhyang University Cheonan Hospital, College of Medicine, Cheonan, Korea.

Abstract

PURPOSE: Survivin is a member of the inhibitor of apoptosis (IAP) protein family, and it is involved in the regulation of cell division. The over-expression of survivin has been reported to be associated with the parameters for a poor prognosis in most human cancers, including lung, breast, colon, stomach, esophagus, pancreas, etc. In this study, we examined the expression of a member of a novel IAP protein family, survivin, in breast cancer and its association with tumor cell apoptosis and the overall prognosis.
METHODS
80 cases of formalin-fixed paraffin-embedded breast cancer tissue were immunostained with, using polyclonal survivin (Novus Biologicals, Littleton, USA), monoclonal bcl-2 (DAKO, Carpinteria, USA), and monoclonal p53 antibodies (DAKO, Carpinteria, USA). The histochemical method used for the analysis of apoptosis was based on ApopTag. Peroxidase In Situ OligoLigation (ISOL) Apoptosis Detection Kit (CHEMICON International Inc. Temecula, USA).
RESULTS
Immunohistochemical analysis showed that cytoplasmic survivin expression was positive in 43 of 80 cases (53.8%) of breast carcinomas and it was positive for 70% of the cases that showed a bcl-2 expression tumors. Statistical analysis revealed that the survivin expression was correlated with lymph node metastasis, the tumor stage, and the histological grade. Although the survivin expression was not correlated with p53 mutations, the survivin positive cases were associated with a bcl-2 expression (p=0.015) and a reduced apoptotic index (p=0.024). On the Cox proportional hazard model analysis, the apoptotic index was not identified as a significant independent predictor of overall survival (p=0.072), although the patients with a low apoptotic index (<0.2%) had a worse survival rates than those patient in the group with a high apoptotic index (> or =0.2%).
CONCLUSION
The results suggest that apoptosis inhibition of apoptosis by survivin may be a prognostic parameter for a worse outcome in breast carcinoma patients.

Keyword

Breast cancer; Apoptosis; Survivin; bcl-2; p53

MeSH Terms

Antibodies
Apoptosis*
Breast Neoplasms*
Breast*
Cell Division
Colon
Cytoplasm
Esophagus
Humans
Lung
Lymph Nodes
Neoplasm Metastasis
Pancreas
Peroxidase
Prognosis
Proportional Hazards Models
Stomach
Survival Rate
Antibodies
Peroxidase

Figure

  • Fig 1 Immunohistochemical examination for survivin. (A) The tumor cells of infiltrating ductal carcinoma show positive reaction in survivin (×100). (B) The cytoplasm of atypical cells in moderate epithelial hyperplasia shows strong positive reaction in survivin (×100). (C) The metastatic tumor cells of infiltrating ductal carcinoma lymph node show positive reaction in survivin (×100).

  • Fig 2 Histochemical staining for bcl-2 and apoptotic tumor cells. (A) bcl-2 expression in breast cancers (×40). (B) in situ oligiligation reaction (ISOL) for apoptosis (arrows: ×200).

  • Fig 3 Kaplan-Meier survival curve according to cytoplasmic survivin expression (A) and high vs. low Apoptotic Index (B).


Reference

1. Tamm I, Wang Y, Sausville E, Scudiero DA, Vigna N, Oltersdorf T, et al. IAP-family protein survivin inhibits caspase activity and apoptosis induced by Fas(CD95), Bax, caspases, and anti-cancer drugs. Cancer Res. 1998. 58:5315–5320.
2. Jang JH, Kim TY, Kim SY, Baek MJ, Oh MH, Kim EH, et al. Expression of survivin in patients with breast cancer. J Korean Breast Cancer Soc. 2004. 7:236–243.
Article
3. Elston CW, Ellis IO. Pathological prognostic factors in breast cancer. I. The value of histological grade in breast cancer: experience from a large study with long-term folloe-up. Histopathology. 1991. 19:403–410.
Article
4. Kerr JF, Gobe GC, Winterford CM, Harmon BV. Anatomical methods in cell death. Methods Cell Biol. 1995. 46:1–27.
5. Wyllie AH. Apoptosis: Cell death under homeostatic control. Arch Toxicol. 1987. 11:3–10.
Article
6. Palumbo A, Yeh J. Apoptosis as a basic mechanism in the ovarian cycle: follicular atresia and Iuteal regression. J Soc Gynecol Invest. 1995. 2:565–573.
Article
7. Lipponen PK, Aaltomaa S, Kosma VM, Syrjanen K. Apoptosis in breast cancer as related to histopathological charateristics and prognosis. Eur J Cancer. 1994. 30A:2068–2073.
8. Tormanen U, Eerola AK, Rainio P, Vahakangas K, Soini Y, Sormunen R, et al. Enhanced apoptosis predicts shortened survival in non-small cell lung carcinoma. Cancer Res. 1995. 55:5595–5602.
9. Jaattela M. Escaping cell death: Survival proteins in cancer. Exp Cell Res. 1992. 248:30–43.
Article
10. Tsujimoto Y, Finger LR, Yunis J, Nowell PC, Croce CM. Cloning of the chomosome breakpoint of neoplastic B cell with the t(14;18) chromosome translocation. Science. 1984. 226:1097–1099.
Article
11. Yang E, Korsmeyer SJ. Molecular thanatoposis: a discourse on the bcl-2 family and cell death. Blood. 1996. 88:386–401.
12. Cory S. Regulation of lymphocyte survival by the bcl-2 gene family. Annu Rev Immunol. 1995. 13:513–543.
Article
13. Leek RD, Kaklamanis L, Pezzella F, Gatter KC, Harris AL. bcl-2 in normal human breast and carcinoma, associated with estrogen receptorpositive, epidermal growth factor-negative tumors and in situ cancer. Br J Cancer. 1994. 69:135–139.
Article
14. Park SH, Kim H, Song BJ. Down regulation of bcl2 expression in invasive ductal carcinomas is both estrogen and progesterone-receptor dependent and associated with poor prognostic factors. Pathol Oncol Res. 2002. 8:26–30.
Article
15. Castiglione F, Sarotto I, Fontana V, Destefanis M, Venturino A, Ferro S, et al. Bcl2, p53 and clinical outcome in a series of 138 operable breast cancer patients. Anticancer Res. 1999. 19:4555–4563.
16. Ritter JH, Dresler GM, Wick MR. Expression of bcl-2 protein in stage TINOMO non-small cell lung carcinoma. Hum Pathol. 1995. 26:1227–1232.
17. Inada T, Kikuyama S, Ichikawa A, Igarashi S, Ogata Y. Bcl-2 expression as a prognostic factor of survival of gastric carcinoma. Anticancer Res. 1998. 18:2003–2010.
18. Hellemans P, Dam PA, Weyler J, Oosteroma AT, Buytaert P, Marck EV. Prognostic value of bcl-2 expression in invasive breast cancer. Br J Cancer. 1995. 72:354–360.
Article
19. Pezzella F, Turley H, Kuzu I, Tungekar MF, Dunnill Ms, Pierce CB, et al. Bcl-2 proteinin non-small cell lung caricnoma. N Eng J Med. 1993. 329:690–694.
20. Crook NE, Clem RJ, Miller LK. An apoptosis-inhibiting baculovirus gene with a zinc finger-like motif. J Virol. 1993. 67:2168–2174.
Article
21. Birnbaum MJ, Clem RJ, Miller LK. An apoptosis-inhibiting gene from a nuclear polyhedrosis virus encoding a polypeptide with Cys/His sequence motifs. J Vitol. 1994. 69:2521–2528.
Article
22. Deveraux QL, Takahashi R, Salvesen GS, Reed JC. X-linked IAP is a direct inhibitor of cell-death protease. Nature. 1997. 388:300–304.
Article
23. Ambrosini G, Adida C, Altieri DC. A novel anti-apoptosis gene, survivin, expressed in cancer and lymphoma. Nature Med. 1997. 3:917–921.
Article
24. Verdecia MA, Huang H, Dutil E, Kaiser DA, Hunter T, Noel JP. Structure of the human anti-apoptotic protein survivin reveals a dimeric arrangement. Nat Struct Biol. 2002. 7:620–623.
25. Hague A, Moorghen M, Hicks D, Champman M, Paraskeva C. Bcl-2 expression in human colorectal adenomas and carcinomas. Oncogene. 1994. 9:3367–3370.
26. LaCasse EC, Baird S, Korneluk RG, Mackenzie AE. The inhibitor of apoptosis (IAPs) and their emerging role in cancer. Oncogene. 1998. 17:3247–3259.
Article
27. Deveraux QL, Reed JC. IAP family proteing-suppressors of apoptosis. Gene Day. 1999. 12:239–252.
28. Olie RA, Simoes-Wust AP, Baumann B, Leech SH, Fabbro D, Stahel RA, et al. A novel antisense oligonucleotide targeting survivin expression induces apoptosis and sensitizes lung cancer cells to chemotherapy. Cancer Res. 2000. 60:2805–2809.
29. Monzo M, Rosell R, Felip E, A studillo J, Sanchez JJ, Maestre J, et al. A novel anti-apoptosisgene:Re-expression of survivin messenger RNA as a prognosis marker in non-small cell lung cancers. J Clin Oncol. 1999. 17:2100–2104.
30. Adida C, Berrebi D, Peuchmaur M, Reyes-Mugica M, Altieri DC. Anti-apoptosis gene, survivin, and prognosis of neuroblastoma. Lancet. 1998. 351:882–883.
Article
31. Okada E, Murai Y, Matsui K, Isizawa S, Cheng C, Masuda M, et al. Survivin expression in tumor cell nuclei is predictive of a favorable prognosis in gastric cancer patients. Cancer Lett. 2001. 163:109–116.
Article
32. Ito T, Shiraki K, Sugimoto K, Yamanaka T, Fujikawa K, Ito M, et al. Survivin promotes cell proliferation in human hepatocellular carcinoma. Hepatology. 2000. 31:1080–1085.
Article
33. Kennedy SM, O'Driscoll L, Purcell R, Fitz-Simons N, McDermott EW, Hill AD, et al. Prognostic importance of survivin in breast cancer. Br J Cancer. 2003. 88:1077–1083.
Article
34. Kawasaki H, Altieri DC, Lu CD, Toyoda M, Tenjo T, Tanigawa N. Inhibition of apoptosis by survivin predicts shorter survival rates in colorectal cancer. Cancer Res. 1998. 58:5071–5074.
35. Lu CD, Altieri DC, Tanigawa N. Expression of a novel antiapoptosis gene, survivin, correlated with tumor cell apoptosis and p53 accumulation in gastric carcinomas. Cancer Res. 1998. 58:1808–1812.
36. Ruvolo PP, Deng X, May WS. Phosphorylation of Bcl2 and regulation of apoptosis. Leukemia. 2001. 15:515–522.
Article
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