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PSMB8作为直肠癌患者术前放疗反应的候选标志物。

PSMB8 as a Candidate Marker of Responsiveness to Preoperative Radiation Therapy in Rectal Cancer Patients.

作者信息

Ha Ye Jin, Tak Ka Hee, Kim Chan Wook, Roh Seon Ae, Choi Eun Kyung, Cho Dong Hyung, Kim Jeong Hwan, Kim Seon Kyu, Kim Seon Young, Kim Yong Sung, Kim Jin Cheon

机构信息

Department of Surgery, University of Ulsan College of Medicine, Seoul, Korea; Asan Institute for Life Sciences, Asan Medical Center, Seoul, Korea.

Department of Surgery, University of Ulsan College of Medicine, Seoul, Korea.

出版信息

Int J Radiat Oncol Biol Phys. 2017 Aug 1;98(5):1164-1173. doi: 10.1016/j.ijrobp.2017.03.023. Epub 2017 Mar 22.

Abstract

PURPOSE

The ability to predict individual responsiveness to cancer therapy is urgently needed. This is particularly true for patients with locally advanced rectal cancer (LARC) because a large proportion are resistant to preoperative chemoradiation therapy (CRT). In this study, we sought to identify markers that could predict response by comparing the gene expression profiles of the tumors of patients who received preoperative CRT.

METHODS AND MATERIALS

The basal gene expression profiles of tumors from 22 LARC patients who were responders (n=9) and nonresponders (n=13) to preoperative CRT were analyzed using RNA sequencing (RNA-Seq). To validate the RNA-Seq findings, real-time reverse transcriptase polymerase chain reaction (RT-PCR) was performed on tumor samples from an additional 40 LARC patients (n=20 responders; n=20 nonresponders). Candidate genes were stably overexpressed or knocked down in colorectal cancer (CRC) cell lines, and the effect on response to radiation was tested in vitro and also in vivo in a mouse xenograft model.

RESULTS

Eight differentially expressed (>16-fold) genes (B3GALT4, HSPA1B, KRBOX1, PPBP, PPP1R18, PSMB8, SLC39A7, and TAP2) associated with the preoperative CRT response were identified (P<.0005). Among these genes, real-time RT-PCR showed that PSMB8 and SLC39A7 were upregulated in the responsive group of the additional 40 LARC patients. In CRC cell lines, PSMB8 overexpression significantly reduced colony formation and increased the apoptosis-inducing molecules cleaved caspase-3 and cleaved PARP after 6-Gy irradiation. PSMB8 knockdown increased colony formation and decreased caspase-3 activation and cleaved PARP levels after irradiation. SLC39A7 overexpression had no significant effects on irradiated CSC cells. After irradiation of the xenografted mice, tumors that arose from CRC cell line HCT116 overexpressing PSMB8 grew more slowly than did those from HCT116 with vector alone.

CONCLUSION

These results suggest that PSMB8 is a predictive marker of preoperative radiosensitivity in LARC patients. Clinical validation in a larger cohort is now required.

摘要

目的

迫切需要具备预测个体对癌症治疗反应的能力。对于局部晚期直肠癌(LARC)患者而言尤其如此,因为很大一部分患者对术前放化疗(CRT)耐药。在本研究中,我们试图通过比较接受术前CRT患者肿瘤的基因表达谱来鉴定可预测反应的标志物。

方法和材料

使用RNA测序(RNA-Seq)分析了22例术前CRT反应者(n = 9)和无反应者(n = 13)的LARC患者肿瘤的基础基因表达谱。为验证RNA-Seq结果,对另外40例LARC患者(n = 20反应者;n = 20无反应者)的肿瘤样本进行了实时逆转录聚合酶链反应(RT-PCR)。候选基因在结肠直肠癌(CRC)细胞系中稳定过表达或敲低,并在体外以及小鼠异种移植模型中体内测试其对辐射反应的影响。

结果

鉴定出八个与术前CRT反应相关的差异表达(> 16倍)基因(B3GALT4、HSPA1B、KRBOX1、PPBP、PPP1R18、PSMB8、SLC39A7和TAP2)(P <.0005)。在这些基因中,实时RT-PCR显示在另外40例LARC患者的反应组中PSMB8和SLC39A7上调。在CRC细胞系中,PSMB8过表达显著减少集落形成,并在6 Gy照射后增加凋亡诱导分子裂解的caspase-3和裂解的PARP。PSMB8敲低增加集落形成,并降低照射后caspase-3激活和裂解的PARP水平。SLC39A7过表达对照射后的CSC细胞无显著影响。对异种移植小鼠进行照射后,过表达PSMB8的CRC细胞系HCT116产生的肿瘤生长比单独载体的HCT116产生的肿瘤更慢。

结论

这些结果表明PSMB8是LARC患者术前放射敏感性的预测标志物。现在需要在更大队列中进行临床验证。

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