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Title: | BCL-2, in combination with MVP and IGF-1R expression, improves prediction of clinical outcome in complete response cervical carcinoma patients treated by radiochemotherapy | Authors: | Henríquez-Hernández, Luis Alberto Lloret, Marta Pinar, Beatriz Bordón, Elisa Rey, Agustín Lubrano, Amina Lara, Pedro Carlos |
Keywords: | Major Vault Protein Adverse Prognostic-Factor Squamous-Cell Carcinoma Double-Strand Breaks End-Joining Pathway, et al |
Issue Date: | 2011 | Publisher: | 0090-8258 | Journal: | Gynecologic Oncology | Abstract: | Objectives. To investigate whether BCL-2 expression would improve MVP/IGF-1R prediction of clinical outcome in cervix carcinoma patients treated by radiochemotherapy, and suggest possible mechanisms behind this effect.Methods. Fifty consecutive patients, who achieved complete response to treatment, from a whole series of 60 cases suffering from non-metastatic localized cervical carcinoma, were prospectively included in this study from July 1999 to December 2003. Follow-up was closed in January 2011. All patients received pelvic radiation (45-64.80 Gy in 1.8-2 Gy fractions) with concomitant cisplatin at 40 mg/m2/week closes followed by brachytherapy. Oncoprotein expression was studied by immunohistochemistry in paraffin-embedded tumour tissue.Results. No relation was found between BCL-2 and clinicopathological variables. High MVP/IGF-1R/BCL-2 tumour expression was strongly related to poor local and regional disease-free survival (P < 0.0001), distant disease-free survival (P= 0.010), disease-free survival (P < 0.0001), and cause-specific survival (P < 0.0001). NHEJ repair protein Ku70/80 expression was significantly repressed in tumours overexpressing all three oncoproteins (P= 0.047). No differences were observed in proliferation (Ki67 expression) or P53 alteration.Conclusions. BCL-2, MVP, and IGF-1R overexpression were related to poorer clinical outcome in cervical cancer patients who achieved clinical complete response to radiochemotherapy. The NHEJ repair protein Ku70/80 expression could be involved in the regulation of these oncoproteins. (C) 2011 Elsevier Inc. All rights reserved. | URI: | http://hdl.handle.net/10553/43061 | ISSN: | 0090-8258 | DOI: | 10.1016/j.ygyno.2011.05.037 | Source: | Gynecologic Oncology[ISSN 0090-8258],v. 122, p. 585-589 |
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