胃癌组织THBS2和Ki-67表达与临床病理特征及预后的关系

魏 洁, 杜 兴龙, 代 元飞, 薛 松, 何 广思
安徽医科大学附属滁州医院/滁州市第一人民医院肿瘤科

摘要


目的:分析THBS2和Ki-67蛋白在胃癌中的表达及其与临床病理特征和预后的关系。方法:选取2017年1月-2020年12月在安徽医科大学附属滁州医院胃肠外科行胃癌根治性手术的93例患者手术切除标本,采用免疫组化检测THBS2与Ki-67在胃癌及癌旁组织的表达,分析THBS2与Ki-67表达与患者临床病理特征的关系及两者表达的相关性,进一步采用单因素和多因素分析两者对预后影响。结果:THBS2与Ki-67在胃癌组织中的表达高于癌旁组织,两者在胃癌患者中的表达与淋巴结转移、TNM分期相关,而与性别、年龄、肿瘤大小、组织学分级、T分期无关。THBS2与Ki-67表达呈正相关关系。单因素分析显示:淋巴结转移、TNM分期、THBS2表达、Ki-67表达是胃癌患者总生存的影响因素;多因素分析显示:TNM分期及双高表达(THBS2高表达+Ki-67高表达)为胃癌患者预后的独立危险因素。结论:THBS2与Ki-67高表达均与预后不良有关,联合检测有助于更好判断预后。

关键词


胃癌;THBS2;Ki-67;预后

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参考


[1]郑荣寿,张思维,孙可欣,等.2016年中国恶性肿瘤流行情况分析[J].中华肿瘤杂志,2023,45(3):212-220.

[2]Kakeji Y, Ishikawa T, Suzuki S, et al. A retrospective 5-year survival analysis of surgically resected gastric cancer cases from the Japanese Gastric Cancer Association nationwide registry (2001-2013)[J]. Gastric Cancer, 2022, 25(6): 1082-1093.

[3]Liao X, Wang W, Yu B, et al. Thrombospondin-2 acts as a bridge between tumor extracellular matrix and immune infiltration in pancreatic and stomach adenocarcinomas: an integrative pan-cancer analysis[J]. Cancer Cell Int, 2022, 22: 213.

[4]Zhang C, Hu C, Su K, et al. The Integrative Analysis of Thrombospondin Family Genes in Pan-Cancer Reveals that THBS2 Facilitates Gastrointestinal Cancer Metastasis[J]. J Oncol, 2021, 2021: 4405491.

[5]Lu Y, Kong X, Zhong W, et al. Diagnostic, Therapeutic, and Prognostic Value of the Thrombospondin Family in Gastric Cancer[J]. Front Mol Biosci, 2021, 8: 647095.

[6]Zhang S, Yang H, Xiang X, et al. THBS2 is Closely Related to the Poor Prognosis and Immune Cell Infiltration of Gastric Cancer[J]. Front Genet, 2022, 13: 803460.

[7]Ye DM, Xu G, Ma W, Li Y, Luo W, Xiao Y, et al. Significant function and research progress of biomarkers in gastric cancer[J]. Oncol Lett, 2020, 19(1): 17-29.

[8]Chang Z, Gao Y, Chen P, et al. THBS2 promotes gastric cancer progression and stemness via the Notch signaling pathway[J]. Am J Cancer Res, 2024, 14(7): 3433-3450.

[9]Chu XD, Lin ZB, Huang T, et al. Thrombospondin-2 holds prognostic value and is associated with metastasis and the mismatch repair process in gastric cancer[J]. BMC Cancer, 2022, 22: 250.

[10]Shi H, Qi C, Meng L, et al. Bone marrow-derived mesenchymal stem cells promote Helicobacter pylori-associated gastric cancer progression by secreting thrombospondin-2[J]. Cell Prolif, 2021, 54(10): e13114.

[11]Li LZ, Dong J, Fu L, et al. Clinical Value of Serum Thrombospondin-2 Combined with CA19-9 in Early Diagnosis of Gastric Cancer[J]. J Oncol, 2021, 2021: 2483964.

[12]Xiong DD, Zeng CM, Jiang L, et al. Ki-67/MKI67 as a predictive biomarker for clinical outcome in gastric cancer patients: an updated Meta-analysis and systematic review involving 53 studies and 7078 patients[J]. J Cancer, 2019, 10(22): 5339-5354.

[13]Liu C, Tao F, Lu J, et al. Defining nomograms for predicting prognosis of early and late recurrence in gastric cancer patients after radical gastrectomy[J]. Medicine (Baltimore), 2023, 102(42): e35585.

[14]Wang L, Feng L, Liu L, et al. Joint effect of THBS2 and VCAN accelerating the poor prognosis of gastric cancer[J]. Aging (Albany NY), 2023, 15(4): 1343-1357.

[15]Kang B, Camps J, Fan B, et al. Parallel single-cell and bulk transcriptome analyses reveal key features of the gastric tumor microenvironment[J]. Genome Biol, 2022, 23: 265.

[16]Liu J, Zhong L, Deng D, et al. The combined signatures of the tumour microenvironment and nucleotide metabolism-related genes provide a prognostic and therapeutic biomarker for gastric cancer[J]. Sci Rep, 2023, 13: 6622.

[17]Wang J, Liu Z, Lin L, et al. Collagen-related gene expression level predicts the prognosis and immune therapy response[J]. Gastric Cancer, 2023, 26(6): 891-903.


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