>
网站首页期刊介绍通知公告编 委 会投稿须知电子期刊广告合作联系我们
最新消息:
DHX33作为可切除结肠癌患者术后辅助化疗预后标志物的临床研究
作者:刘楠楠  宋珊珊  李凡 
单位:辽宁省健康产业集团阜新矿总医院 消化内科, 辽宁 阜新 123000
关键词:结肠癌 DEAH盒解旋酶33 辅助化疗 根治性切除 预后 
分类号:R735.3;R453
出版年·卷·期(页码):2022·41·第五期(660-667)
摘要:

目的:分析可切除结肠癌(CC)患者肿瘤组织DEAH盒解旋酶33(DHX33)表达作为术后辅助化疗(ACT)预后标志物的临床意义。方法:选取2014年1月至2018年9月期间在我院经根治性手术切除的CC患者215例,所有患者术后接受标准方案的ACT。采用免疫组织化学法分析肿瘤组织和癌旁正常组织中DHX33蛋白表达。以无病生存时间及总生存时间作为主要观察终点。结果:与癌旁正常组织(17.67%,38/215)相比,53.95%(116/215)的肿瘤组织样本中DHX33呈高表达(χ2=61.545,P<0.001)。与DHX33低表达亚组相比,DHX33高表达亚组CC组织微卫星不稳定比例(P=0.020)、cTNM Ⅲ~ⅣA期比例(P=0.025)及癌旁正常组织DHX33蛋白高表达比例(P=0.049)更高。Kaplan-Meier分析显示,DHX33低表达者无病生存时间和总生存时间更长(χ2分别为12.566、13.986,均P<0.001)。单因素及多因素COX回归分析的结果显示,CC组织中DHX33蛋白高表达是影响手术+ACT治疗后复发(OR为2.321,95%CI 1.359~3.962,P=0.002)和远期死亡(OR为3.327,95%CI 1.635~6.769,P=0.001)的独立危险因素。结论:原发性肿瘤组织中DHX33高表达可能是CC患者根治性手术+ACT治疗后复发和死亡的有效预测因子。

Objective: To analyze the clinical value of DEAH-box helicase 33(DHX33) in the tumor tissues of patients with resectable colon cancer(CC) as a prognostic marker of postoperative adjuvant chemotherapy. Methods: A total of 215 patients with CC surgery in our hospital from January 2014 to September 2018 were selected, who were treated with postoperative adjuvant chemotherapy. The DHX33 expression was analyzed by immunohistochemistry. Disease-free survival and overall survival were the main endpoint. Results: Compared with normal adjacent tissues(17.67%, 38/215), 53.95%(116/215) samples showed high expression of DHX33 in tumor tissues(χ2=61.545, P<0.001). Compared with the DHX33 low expression subgroup, the proportion of microsatellite instability(P=0.020), the proportion of cTNM phase Ⅲ-ⅣA(P=0.025) in CC tissues and the proportion of DHX33 protein high expression in normal adjacent tissues(P=0.049) were higher in the DHX33 high expression subgroup. Kaplan-Meier analysis showed that the CC patients with lower DHX33 expression had longer disease-free survival and overall survival timesχ2=12.566, 13.986, P<0.001). Univariate and multivariate COX regression analysis showed that the high expression of DHX33 protein in CC tissue was an independent risk factor for recurrence(OR=2.321, 95%CI 1.359-3.962, P=0.002) and long-term death(OR=3.327, 95%CI 1.635-6.769, P=0.001). Conclusion: The high expression of DHX33 in primary tumor tissue may be an effective predictor of recurrence or death in CC patients after radical resection +ACT treatment.

参考文献:

[1] BENDER U, RHO Y S, BARRERA I, et al.Adjuvant therapy for stages II and III colon cancer:risk stratification, treatment duration, and future directions[J].Curr Oncol, 2019, 26(Suppl 1):S43-S52.
[2] 聂双发, 费建东, 李磊, 等.结肠癌根治术后辅助化疗的疗效及影响预后的多因素分析[J].中国老年学杂志, 2018, 38(2):352-354.
[3] 成秉禄, 杨天敬, 周毅, 等.WT1蛋白表达与结肠癌患者病理特征及预后相关性的研究[J].癌症, 2021, 40(8):360-366.
[4] 何兴政, 张传国, 蔡玉建.完整结肠系膜切除术治疗结肠癌患者效果及对术后恢复质量的影响[J].中国医药科学, 2022, 12(4):150-153.
[5] WANG X, GE W, ZHANG Y.Recombinant DHX33 protein possesses dual DNA/RNA helicase activity[J].Biochemistry, 2019, 58(4):250-258.
[6] LIU Y, LU N, YUAN B, et al.The interaction between the helicase DHX33 and IPS-1 as a novel pathway to sense double-stranded RNA and RNA viruses in myeloid dendritic cells[J].Cell Mol Immunol, 2014, 11(1):49-57.
[7] 肖毅, 徐徕, 陆君阳.根治性右半结肠癌淋巴结清扫范围的探讨[J].中华外科杂志, 2016, 54(6):408-412.
[8] PANARELLI N C, HAMMER S T G, LIN J, et al.Reproducibility of AJCC criteria for classifying deeply invasive colon cancers is suboptimal for consistent cancer staging[J].Am J Surg Pathol, 2020, 44(10):1381-1388.
[9] WANG X, DUANMU J, FU X, et al.Analyzing and validating the prognostic value and mechanism of colon cancer immune microenvironment[J].J Transl Med, 2020, 18(1):324-337.
[10] LIU H, MA L, WANG L, et al.MicroRNA-937 is overexpressed and predicts poor prognosis in patients with colon cancer[J].Diagn Pathol, 2019, 14(1):136-143.
[11] 樊小群, 李欢, 朱华雄, 等.Mir-335-5p靶向G6PD对结肠癌细胞增殖、凋亡的影响[J].中国应用生理学杂志, 2021, 37(4):402-406.
[12] CHEN P H, WU Y Y, LEE C H, et al.Uracil-tegafur vs fluorouracil as postoperative adjuvant chemotherapy in Stage II and III colon cancer:a nationwide cohort study and meta-analysis[J].Medicine (Baltimore), 2021, 100(18):e25756-e25763.
[13] ZHOU W, YANG F, PENG J, et al.High pretreatment serum CA19-9 level predicts a poor prognosis for patients with stage Ⅲ colon cancer after curative resection and adjuvant chemotherapy[J].J Cancer, 2019, 10(16):3810-3818.
[14] 戈雨桐, 哈文韬, 魏晓为, 等.基于列线图探索脑内皮黏附分子表达水平在结肠癌预后预测中的作用[J].中国肿瘤生物治疗杂志, 2022, 29(5):456-463.
[15] 龚海峰, 王浩, 张玉波, 等.结肠癌中LZTS1和CDK1表达与术后辅助化疗敏感性的关系[J].现代肿瘤医学, 2020, 28(14):2452-2456.
[16] ZHANG Y, YOU J, WANG X, et al.The DHX33 RNA helicase promotes mRNA translation initiation[J].Mol Cell Biol, 2015, 35(17):2918-2931.
[17] ZHANG Y, SAPORITA A J, WEBER J D.P19ARF and RasV12 offer opposing regulation of DHX33 translation to dictate tumor cell fate[J].Mol Cell Biol, 2013, 33(8):1594-1607.
[18] WANG H, YU J, WANG X, et al.The RNA helicase DHX33 is required for cancer cell proliferation in human glioblastoma and confers resistance to PI3K/mTOR inhibition[J].Cell Signal, 2019, 54(2):170-178.
[19] WANG J, FENG W, YUAN Z, et al.DHX33 interacts with AP-2β to regulate Bcl-2 gene expression and promote cancer cell survival[J].Mol Cell Biol, 2019, 39(17):e00017-19.
[20] WANG X, FENG W, PENG C, et al.Targeting RNA helicase DHX33 blocks Ras-driven lung tumorigenesis in vivo[J].Cancer Sci, 2020, 111(10):3564-3575.
[21] YUAN B, WANG X, FAN C, et al.DHX33 transcriptionally controls genes involved in the cell cycle[J].Mol Cell Biol, 2016, 36(23):2903-2917.

服务与反馈:
文章下载】【发表评论】【查看评论】【加入收藏
提示:您还未登录,请登录!点此登录
您是第 414636 位访问者


copyright ©《东南大学学报(医学版)》编辑部
联系电话:025-83272481 83272483
电子邮件:
bjb@pub.seu.edu.cn

苏ICP备09058364