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小窝蛋白-1过表达与侵袭性前列腺癌复发相关。

Caveolin-1 overexpression is associated with aggressive prostate cancer recurrence.

作者信息

Karam Jose A, Lotan Yair, Roehrborn Claus G, Ashfaq Raheela, Karakiewicz Pierre I, Shariat Shahrokh F

机构信息

Department of Urology, University of Texas Southwestern Medical Center, Dallas, TX 75390-9110, USA.

出版信息

Prostate. 2007 May 1;67(6):614-22. doi: 10.1002/pros.20557.

Abstract

BACKGROUND

Caveolin-1 protein suppresses apoptotic cell death in prostate cancer. The objectives of this study were to investigate the association of Caveolin-1 expression with established features of prostate cancer as well as overall and aggressive disease recurrence in patients treated with radical prostatectomy (RP).

METHODS

Caveolin-1 immunostaining was performed on a tissue microarray containing prostatectomy specimen cores from 232 consecutive patients treated with RP for clinically localized prostatic adenocarcinoma. Caveolin-1 over-expression was defined as more than 50% of cells staining positively for Caveolin-1. Patients were categorized as having features of aggressive disease recurrence if they had a positive metastatic work-up, post-recurrence PSA doubling time less than 10 months, and/or failure to respond to local salvage radiation therapy.

RESULTS

Seventy patients (30.2%) exhibited over-expression of Caveolin-1. Caveolin-1 over-expression was associated with higher pathologic Gleason sum (P=0.038) and higher pre-operative PSA level (P=0.024). Patients with Caveolin-1 over-expression were at increased risk of PSA recurrence after surgery (P=0.023) in univariate but not in standard post-operative multivariate analysis. However, patients with Caveolin-1 over-expression were at increased risk of aggressive prostate cancer recurrence in both univariate and multivariate analysis (P<0.001 and P=0.001, respectively).

CONCLUSIONS

Over-expression of Caveolin-1 was associated with established features of prostate cancer and aggressive PSA recurrence. Caveolin-1 might help identify patients at high risk of developing aggressive prostate cancer recurrence, thus allowing selection of patients who might benefit from early systemic therapeutic intervention.

摘要

背景

小窝蛋白-1蛋白可抑制前列腺癌中的凋亡细胞死亡。本研究的目的是探讨小窝蛋白-1表达与前列腺癌既定特征以及接受根治性前列腺切除术(RP)治疗的患者总体和侵袭性疾病复发之间的关联。

方法

对包含232例因临床局限性前列腺腺癌接受RP治疗的患者的前列腺切除标本芯的组织微阵列进行小窝蛋白-1免疫染色。小窝蛋白-1过表达定义为超过50%的细胞对小窝蛋白-1染色呈阳性。如果患者转移检查呈阳性、复发后PSA倍增时间小于10个月和/或对局部挽救性放射治疗无反应,则被归类为具有侵袭性疾病复发特征。

结果

70例患者(30.2%)表现出小窝蛋白-1过表达。小窝蛋白-1过表达与更高的病理Gleason评分(P=0.038)和更高的术前PSA水平(P=0.024)相关。在单变量分析中,小窝蛋白-1过表达的患者术后PSA复发风险增加(P=0.023),但在标准术后多变量分析中未增加。然而,在单变量和多变量分析中,小窝蛋白-1过表达的患者侵袭性前列腺癌复发风险均增加(分别为P<0.001和P=0.001)。

结论

小窝蛋白-1过表达与前列腺癌既定特征和侵袭性PSA复发相关。小窝蛋白-1可能有助于识别发生侵袭性前列腺癌复发高风险患者,从而允许选择可能从早期全身治疗干预中获益的患者。

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