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PTEN 肿瘤抑制因子在弥漫性大 B 细胞淋巴瘤中的预后作用不如 P53 肿瘤抑制因子。

PTEN tumor suppressor plays less prognostic role than P53 tumor suppressor in diffuse large B-cell lymphoma.

机构信息

Department of Internal Medicine, Henan Provincial Cancer Hospital, Henan Provincial Institute of Cancer, Zhengzhou, Henan Province, China.

出版信息

Leuk Lymphoma. 2010 Sep;51(9):1692-8. doi: 10.3109/10428194.2010.502584.

Abstract

The phosphatase and tensin homolog deleted on chromosome 10 (PTEN) and P53 tumor suppressors are among the most commonly inactivated or mutated genes in human cancers, whose pathways cross-talk and interact in a complementary mode. In order to understand their roles and relationship in diffuse large B-cell lymphoma (DLBCL), we examined their expression and evaluated their prognostic significance in 62 patients with DLBCL treated with standard chemotherapy. Results showed that PTEN protein was lost in 23 (37.1%) cases, and the loss was associated with the activation of PI3K/AKT pathway, but was not associated with patient's clinical outcome. P53 mutation protein was detected in 30 (48.4%) cases and was associated with poor survival. Results of multivariate analysis showed that P53 mutation but not PTEN loss is associated with short survival in patients with DLBCL. PTEN status has no effect on P53 mutation-associated poor survival. We conclude that PTEN may play less prognostic role than P53 and that P53 mutation protein should be considered as a predictive factor of the need for a more aggressive therapy in patients with DLBCL who express P53.

摘要

第 10 号染色体缺失的磷酸酶及张力蛋白同源物(PTEN)和 P53 肿瘤抑制因子是人类癌症中最常失活或突变的基因之一,它们的通路以互补的方式相互作用和交叉对话。为了了解它们在弥漫性大 B 细胞淋巴瘤(DLBCL)中的作用和关系,我们检测了 62 例接受标准化疗的 DLBCL 患者中它们的表达情况,并评估了它们的预后意义。结果表明,23 例(37.1%)患者的 PTEN 蛋白缺失,这种缺失与 PI3K/AKT 通路的激活有关,但与患者的临床结局无关。30 例(48.4%)患者检测到 P53 突变蛋白,与不良生存相关。多因素分析结果显示,P53 突变而非 PTEN 缺失与 DLBCL 患者的短生存期相关。PTEN 状态对 P53 突变相关不良预后无影响。我们的结论是,PTEN 可能比 P53 发挥更小的预后作用,在表达 P53 的 DLBCL 患者中,P53 突变蛋白应被视为更积极治疗需求的预测因子。

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