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Deciphering tertiary lymphoid structure heterogeneity reveals prognostic signature and therapeutic potentials for colorectal cancer: a multicenter retrospective cohort study.
Lei, Jia-Xin; Wang, Runxian; Hu, Chuling; Lou, Xiaoying; Lv, Min-Yi; Li, Chenghang; Gai, Baowen; Wu, Xiao-Jian; Dou, Ruoxu; Cai, Du; Gao, Feng.
Afiliação
  • Lei JX; Department of General Surgery (Colorectal Surgery), The Sixth Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong Province, 510655, China.
  • Wang R; School of Medicine, Shenzhen Campus of Sun Yat-Sen University, Shenzhen, Guangdong Province, 518107, China.
  • Hu C; Department of Gastrointestinal Surgery, The Fifth Affiliated Hospital of Sun Yat-sen University, Zhuhai, Guangdong Province, 519000, P. R. China.
  • Lou X; Department of General Surgery (Colorectal Surgery), The Sixth Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong Province, 510655, China.
  • Lv MY; Guangdong Provincial Key Laboratory of Colorectal and Pelvic Floor Diseases, The Sixth Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong Province, 510655, China.
  • Li C; Biomedical Innovation Center, The Sixth Affiliated Hospital, Sun Yat-sen University.
  • Gai B; Department of Pathology, The Sixth Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
  • Wu XJ; Department of General Surgery (Colorectal Surgery), The Sixth Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong Province, 510655, China.
  • Dou R; Guangdong Provincial Key Laboratory of Colorectal and Pelvic Floor Diseases, The Sixth Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong Province, 510655, China.
  • Cai D; Biomedical Innovation Center, The Sixth Affiliated Hospital, Sun Yat-sen University.
  • Gao F; Artificial Intelligence Thrust, The Hong Kong University of Science and Technology, Guangzhou, 510030, China.
Int J Surg ; 2024 Jun 04.
Article em En | MEDLINE | ID: mdl-38833363
ABSTRACT

BACKGROUND:

Tertiary lymphoid structures (TLSs) exert a crucial role in the tumor microenvironment (TME), impacting tumor development, immune escape, and drug resistance. Nonetheless, the heterogeneity of TLSs in colorectal cancer (CRC) and their impact on prognosis and treatment response remain unclear.

METHODS:

We collected genome, transcriptome, clinicopathological information, and digital pathology images from multiple sources. An unsupervised clustering algorithm was implemented to determine diverse TLS patterns in CRC based on the expression levels of 39 TLS signature genes (TSGs). Comprehensive explorations of heterogeneity encompassing mutation landscape, TME, biological characteristics, response to immunotherapy, and drug resistance were conducted using multi-omics data. TLSscore was then developed to quantitatively assess TLS patterns of individuals for further clinical applicability.

RESULTS:

Three distinct TLS patterns were identified in CRC. Cluster 1 exhibited upregulation of proliferation-related pathways, high metabolic activity, and intermediate prognosis, while Cluster 2 displayed activation of stromal and carcinogenic pathways and a worse prognosis. Both Cluster 1 and Cluster 2 may potentially benefit from adjuvant chemotherapy. Cluster 3, characterized by the activation of immune regulation and activation pathways, demonstrated a favorable prognosis and enhanced responsiveness to immunotherapy. We subsequently employed a regularization algorithm to construct the TLSscore based on 9 core genes. Patients with lower TLSscore trended to prolonged prognosis and a more prominent presence of TLSs, which may benefit from immunotherapy. Conversely, those with higher TLSscore exhibited increased benefits from adjuvant chemotherapy.

CONCLUSIONS:

We identified distinct TLS patterns in CRC and characterized their heterogeneity through multi-omics analyses. The TLSscore held promise for guiding clinical decision-making and further advancing the field of personalized medicine in CRC.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article