Intratumoral microbiome is associated with gastric cancer prognosis and therapy efficacy

被引:12
作者
Wang, Gangjian [1 ]
Wang, Haojie [2 ,3 ]
Ji, Xin [4 ]
Wang, Tong [5 ]
Zhang, Ye [5 ]
Jiang, Wenjie [6 ,7 ]
Meng, Lin [8 ]
Wu, Hua-Jun [2 ,9 ,10 ]
Xing, Xiaofang [1 ,11 ]
Ji, Jiafu [4 ,11 ]
机构
[1] Peking Univ Canc Hosp & Inst, Div Gastrointestinal Canc Translat Res Lab, 52 Fu-Cheng Rd, Beijing 100142, Peoples R China
[2] Peking Univ Canc Hosp & Inst, Minist Educ, Key Lab Carcinogenesis & Translat Res, Beijing, Peoples R China
[3] Chinese Acad Sci, Inst Genet & Dev Biol, Beijing, Peoples R China
[4] Peking Univ Canc Hosp & Inst, Minist Educ, Div Gastrointestinal Canc Ctr, Key Lab Carcinogenesis & Translat Res, 52 Fu Cheng Rd, Beijing 100142, Peoples R China
[5] Nanjing Med Univ, Affiliated Wuxi Peoples Hosp, Dept Gen Surg, Wuxi, Jiangsu, Peoples R China
[6] Peking Univ Third Hosp, Dept Cardiol, Beijing, Peoples R China
[7] Peking Univ Third Hosp, Inst Vasc Med, Beijing, Peoples R China
[8] Peking Univ Canc Hosp & Inst, Minist Educ, Dept Biochem & Mol Biol, Key Lab Carcinogenesis & Translat Res, Beijing, Peoples R China
[9] Peking Univ, Sch Basic Med Sci, Dept Biomed Informat, Hlth Sci Ctr, Beijing, Peoples R China
[10] Peking Univ, Inst Adv Clin Med, Ctr Precis Med Multiom Res, 8 Life Pk Rd 12-B 1-F, Beijing 100142, Peoples R China
[11] Peking Univ Canc Hosp & Inst, Gastrointestinal Canc Ctr, State Key Lab Holist Integrat Management Gastroint, Beijing Key Lab Carcinogenesis & Translat Res, Beijing, Peoples R China
基金
中国国家自然科学基金; 国家高技术研究发展计划(863计划);
关键词
Prognosis; adjuvant chemotherapy; immunotherapy; microbial subtype; MOLECULAR ANALYSIS; CELLS; INFILTRATION; CHEMOTHERAPY; METABOLITES; LINKS;
D O I
10.1080/19490976.2024.2369336
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The role of the intratumoral microbiome in gastric cancer (GC) has not been comprehensively assessed. Here, we explored the relationship between the microbial community and GC prognosis and therapy efficacy. Several cancer-associated microbial characteristics were identified, including increased alpha-diversity, differential beta-diversity, and decreased Helicobacter pylori abundance. After adjusting for clinical features, prognostic analysis revealed 2 phyla, 14 genera, and 5 species associated with the overall survival of patients with GC. Additionally, 2 phyla, 14 genera, and 6 species were associated with adjuvant chemotherapy (ACT) efficacy in patients with stage II - III GC. Furthermore, we classified GC microbiome structures into three microbial subtypes (MS1, MS2 and MS3) with distinguishing features. The MS1 subtype exhibited high immune activity and enrichment of microbiota related to immunotherapy and butyric acid-producing, as well as potential benefits in immunotherapy. MS2 featured the highest alpha-diversity and activation of the TFF pathway, MS3 was characterized by epithelial-mesenchymal transition and was associated with poor prognosis and reduced ACT efficacy. Collectively, the results of this study provide valuable insights into the microbial characteristics associated with GC prognosis and therapy efficacy.
引用
收藏
页数:17
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