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可溶性 CD146 是透明细胞肾细胞癌不良预后和舒尼替尼疗效的预测标志物。

Soluble CD146 is a predictive marker of pejorative evolution and of sunitinib efficacy in clear cell renal cell carcinoma.

机构信息

Centre Scientifique de Monaco, Biomedical Department, 8 Quai Antoine Ier, MC-98000 Monaco, Principality of Monaco.

Aix Marseille Univ, INSERM 1263, INRA 1260, C2VN, Marseille, France.

出版信息

Theranostics. 2018 Mar 28;8(9):2447-2458. doi: 10.7150/thno.23002. eCollection 2018.

Abstract

The objective of the study was to use CD146 mRNA to predict the evolution of patients with non-metastatic clear cell renal cell carcinoma (M0 ccRCC) towards metastatic disease, and to use soluble CD146 (sCD146) to anticipate relapses on reference treatments by sunitinib or bevacizumab in patients with metastatic ccRCC (M1). : A retrospective cohort of M0 patients was used to determine the prognostic role of intra-tumor CD146 mRNA. Prospective multi-center trials were used to define plasmatic sCD146 as a predictive marker of sunitinib or bevacizumab efficacy for M1 patients. : High tumor levels of CD146 mRNA were linked to shorter disease-free survival (DFS) and overall survival (OS). ccRCC patients from prospective cohorts with plasmatic sCD146 variation <120% following the first cycle of sunitinib treatment had a longer progression-free survival (PFS) and OS. The plasmatic sCD146 variation did not correlate with PFS or OS for the bevacizumab-based treatment. resistant cells to sunitinib expressed high levels of CD146 mRNA and protein in comparison to sensitive cells. Moreover, recombinant CD146 protected cells from the sunitinib-dependent decrease of cell viability. : CD146/sCD146 produced by tumor cells is a relevant biological marker of ccRCC aggressiveness and relapse on sunitinib treatment.

摘要

本研究旨在通过检测 CD146mRNA 预测非转移性透明细胞肾细胞癌(M0ccRCC)患者向转移性疾病的进展,并通过检测可溶性 CD146(sCD146)预测转移性 ccRCC(M1)患者对舒尼替尼或贝伐单抗标准治疗的复发情况:利用 M0 患者的回顾性队列确定肿瘤内 CD146mRNA 的预后作用。前瞻性多中心试验用于定义血浆 sCD146 作为 M1 患者舒尼替尼或贝伐单抗疗效的预测标志物。肿瘤中 CD146mRNA 水平高与无病生存期(DFS)和总生存期(OS)缩短相关。在接受舒尼替尼治疗的第一个周期后,血浆 sCD146 变化<120%的前瞻性队列中的 ccRCC 患者,其无进展生存期(PFS)和 OS 更长。对于基于贝伐单抗的治疗,血浆 sCD146 变化与 PFS 或 OS 均无相关性。与敏感细胞相比,对舒尼替尼耐药的细胞表达高水平的 CD146mRNA 和蛋白。此外,重组 CD146 可保护细胞免受舒尼替尼依赖的细胞活力下降。肿瘤细胞产生的 CD146/sCD146 是 ccRCC 侵袭性和舒尼替尼治疗复发的相关生物学标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd94/5928901/32c541e53fc5/thnov08p2447g001.jpg

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