Literature DB >> 8920796

Expression of p53 and apoptosis of tumor cells in locally advanced cervical carcinoma after cisplatin based neoadjuvant chemotherapy.

G G Garzetti1, A Ciavattini, M Provinciali, G Di Stefano, G Lucarini, G Goteri, G Biagini.   

Abstract

Various chemoantiblastic agents cause DNA damage followed by apoptotic cell death through the activation of the p53 suppressor gene. The aim of our study was to evaluate the relationship between p53 protein expression, apoptosis of autologous tumor cells, and clinical response to neoadjuvant chemotherapy in patients with cervical carcinoma. Our study included 14 women with stage II squamous cervical carcinoma who had been admitted to the Institute of Gynecology and Obstetrics, Ancona University, between January 1990 and December 1995. The patients received neoadjuvant combination chemotherapy, consisting of three cycles of cisplatin (80 mg/m2) and bleomycin (30 mg/m2). After chemotherapy, radical surgery was performed. Bioptic specimens were obtained from cervical tumors before and after chemotherapy, and processed for DNA staining and apoptosis, and immunohistochemical staining with a monoclonal antibody against p53. Ten patients (71.4%) showed a clinical response (2 complete, and 8 partial), while of the remaining 4 cases (28.6%) 3 had no change and 1 showed progression after neoadjuvant combination chemotherapy. A significant relationship was observed between the overexpression of p53 and sensitivity to chemotherapy; responder patients showed a higher frequency of p53 positive cells than non-responders (p = .05). A significant direct relationship was observed between p53 protein immunostaining and apoptosis of tumor cells both before (p = .02) and after (p = .01) chemotherapy. Our study seems to define the relationship between p53 expression and sensitivity to cisplatin based chemotherapy in locally advanced cervical carcinoma, supporting the notion that the cytotoxic action of cisplatin can activate p53 mediated apoptosis. However, the limited number of patients in our series does not permit judgement on the clinical implications of the expression of p53 in patients undergoing neoadjuvant combination chemotherapy for locally advanced cervical carcinoma.

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Year:  1996        PMID: 8920796

Source DB:  PubMed          Journal:  Anticancer Res        ISSN: 0250-7005            Impact factor:   2.480


  5 in total

Review 1.  Molecular mechanisms of cisplatin resistance in cervical cancer.

Authors:  Haiyan Zhu; Hui Luo; Wenwen Zhang; Zhaojun Shen; Xiaoli Hu; Xueqiong Zhu
Journal:  Drug Des Devel Ther       Date:  2016-06-07       Impact factor: 4.162

2.  HP1γ Sensitizes Cervical Cancer Cells to Cisplatin through the Suppression of UBE2L3.

Authors:  Sang Ah Yi; Go Woon Kim; Jung Yoo; Jeung-Whan Han; So Hee Kwon
Journal:  Int J Mol Sci       Date:  2020-08-19       Impact factor: 5.923

Review 3.  Biological and clinical aspects of HPV-related cancers.

Authors:  Klaudia Anna Szymonowicz; Junjie Chen
Journal:  Cancer Biol Med       Date:  2020-12-15       Impact factor: 4.248

4.  The Distinct Roles of LKB1 and AMPK in p53-Dependent Apoptosis Induced by Cisplatin.

Authors:  Tatsuya Shimada; Yohsuke Yabuki; Takuya Noguchi; Mei Tsuchida; Ryuto Komatsu; Shuhei Hamano; Mayuka Yamada; Yusuke Ezaki; Yusuke Hirata; Atsushi Matsuzawa
Journal:  Int J Mol Sci       Date:  2022-09-02       Impact factor: 6.208

Review 5.  The Relationship Between Actin Cytoskeleton and Membrane Transporters in Cisplatin Resistance of Cancer Cells.

Authors:  Takahiro Shimizu; Takuto Fujii; Hideki Sakai
Journal:  Front Cell Dev Biol       Date:  2020-10-27
  5 in total

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