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基于顺铂的新辅助化疗后局部晚期宫颈癌中p53的表达及肿瘤细胞凋亡

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

作者信息

Garzetti G G, Ciavattini A, Provinciali M, Di Stefano G, Lucarini G, Goteri G, Biagini G

机构信息

Institute of Obstetrics and Gynecology, Università degli Studi di Ancona, Italy.

出版信息

Anticancer Res. 1996 Sep-Oct;16(5B):3229-34.

PMID:8920796
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.

摘要

多种化疗药物会导致DNA损伤,随后通过激活p53抑癌基因引发凋亡性细胞死亡。我们研究的目的是评估p53蛋白表达、自体肿瘤细胞凋亡与宫颈癌患者新辅助化疗临床反应之间的关系。我们的研究纳入了1990年1月至1995年12月期间入住安科纳大学妇产科研究所的14例II期宫颈鳞癌女性患者。患者接受新辅助联合化疗,包括三个周期的顺铂(80mg/m²)和博来霉素(30mg/m²)。化疗后进行根治性手术。在化疗前后从宫颈肿瘤获取活检标本,进行DNA染色、凋亡检测以及用抗p53单克隆抗体进行免疫组化染色。10例患者(71.4%)显示出临床反应(2例完全缓解,8例部分缓解),而其余4例患者(28.6%)中,3例无变化,1例在新辅助联合化疗后病情进展。观察到p53过表达与化疗敏感性之间存在显著关系;有反应的患者p53阳性细胞频率高于无反应者(p = 0.05)。在化疗前(p = 0.02)和化疗后(p = 0.01),均观察到p53蛋白免疫染色与肿瘤细胞凋亡之间存在显著的直接关系。我们的研究似乎明确了局部晚期宫颈癌中p53表达与对顺铂为基础的化疗敏感性之间的关系,支持顺铂的细胞毒性作用可激活p53介导的凋亡这一观点。然而,我们系列研究中的患者数量有限,无法对局部晚期宫颈癌接受新辅助联合化疗患者中p53表达的临床意义做出判断。

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