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Translationally Controlled Tumor Protein in Prostatic Adenocarcinoma: Correlation with Tumor Grading and Treatment-Related Changes

机译:前列腺腺癌中的翻译控制肿瘤蛋白:与肿瘤分级和治疗相关变化的相关性

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摘要

Prostate cancer is the second leading cause of cancer-related death. The androgen deprivation therapy is the standard treatment for advanced stages. Unfortunately, virtually all tumors become resistant to androgen withdrawal. The progression to castration-resistance is not fully understood, although a recent paper has suggested translationally controlled tumor protein to be implicated in the process. The present study was designed to investigate the role of this protein in prostate cancer, focusing on the correlation between its expression level with tumor differentiation and response to treatment. We retrieved 292 prostatic cancer specimens; of these 153 had been treated only by radical prostatectomy and 139 had undergone radical prostatectomy after neoadjuvant treatment with combined androgen blockade therapy. Non-neoplastic controls were represented by 102 prostatic peripheral zone specimens. In untreated patients, the expression of the protein, evaluated by RT-qPCR and immunohistochemistry, was significantly higher in tumor specimens than in non-neoplastic control, increasing as Gleason pattern and score progressed. In treated prostates, the staining was correlated with the response to treatment. An association between protein expression and the main clinicopathological factors involved in prostate cancer aggressiveness was identified. These findings suggest that the protein may be a promising prognostic factor and a target for therapy.
机译:前列腺癌是癌症相关死亡的第二个主要原因。雄激素剥夺疗法是高级阶段的标准治疗。不幸的是,几乎所有肿瘤都对雄激素戒断性抵抗力。阉割抵抗力的进展尚不完全明白,尽管最近的一篇论文提出了平移控制的肿瘤蛋白,以涉及该过程。本研究旨在探讨该蛋白质在前列腺癌中的作用,重点关注其表达水平与肿瘤分化与治疗的反应之间的相关性。我们检索了292个前列腺癌标本;在这些153中仅受到自由基前列腺切除术治疗的,139在Neoadjuvant治疗后的组合雄激素封闭治疗后经过根治性前列腺切除术。非肿瘤对照由102个前列腺外周区标本表示。在未经治疗的患者中,蛋白质的表达,通过RT-QPCR和免疫组织化学评估,肿瘤标本显着高于非肿瘤控制,随着GLEASOS的模式和得分进展而增加。在治疗的前列腺中,染色与对治疗的反应相关。鉴定了蛋白质表达与参与前列腺癌侵袭性的主要临床病理因素之间的关联。这些发现表明蛋白质可能是有希望的预后因子和治疗靶标。

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