Cancer Stem Cells in Human Gastrointestinal and Hepatic Cancers

Gastrointestinal cancers, including gastric, hepatic, and colorectal cancers, represent a major public health problem globally. Although the 5-year survival rate of gastrointestinal tumors has been greatly improved due to the progress of diagnostic and therapeutic strategies, therapeutic resistance and distant metastasis remain the leading causes of cancer-related death in patients with gastrointestinal tumors. Cancer stem cells (CSCs) are a population of self-renewal cells with extremely strong carcinogenic potency, contributing to the progression, metastasis, and therapeutic resistance of gastrointestinal tumors. It is generally accepted that gastrointestinal CSCs have the characteristics of self-renewal, pluripotency, tumorigenicity, metastatic potential, and therapeutic resistance. Hence, understanding the behaviors of gastrointestinal CSCs is important for characterizing the stemness landscapes of gastrointestinal tumors and developing promising strategies for the treatment of gastrointestinal tumors. This review aims to discuss the basic characteristics of gastrointestinal CSCs, existing approaches to define and isolate CSCs, and canonical molecular pathways involved in the regulation of gastrointestinal CSCs. More importantly, potential strategies targeting gastrointestinal CSCs are proposed to overcome the limitations of current therapies.

Authors

Institutions

Publication Details

Journal
MedComm
Published
2025-12-01
DOI
https://doi.org/10.1002/mco2.70513
Primary Topic
Cancer Cells and Metastasis
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Cancer Stem Cells in Human Gastrointestinal and Hepatic Cancers

Fu Peng, Jiawen Bu, Yu Zhang, Xudong Zhu et al.
MedComm
Cancer Cells and Metastasis
article

Cancer Stem Cells in Human Gastrointestinal and Hepatic Cancers

Fu Peng, Jiawen Bu, Yu Zhang, Xudong Zhu, Hong Zhang, Lu Yu, Mingming Cui
article en

Abstract

Gastrointestinal cancers, including gastric, hepatic, and colorectal cancers, represent a major public health problem globally. Although the 5-year survival rate of gastrointestinal tumors has been greatly improved due to the progress of diagnostic and therapeutic strategies, therapeutic resistance and distant metastasis remain the leading causes of cancer-related death in patients with gastrointestinal tumors. Cancer stem cells (CSCs) are a population of self-renewal cells with extremely strong carcinogenic potency, contributing to the progression, metastasis, and therapeutic resistance of gastrointestinal tumors. It is generally accepted that gastrointestinal CSCs have the characteristics of self-renewal, pluripotency, tumorigenicity, metastatic potential, and therapeutic resistance. Hence, understanding the behaviors of gastrointestinal CSCs is important for characterizing the stemness landscapes of gastrointestinal tumors and developing promising strategies for the treatment of gastrointestinal tumors. This review aims to discuss the basic characteristics of gastrointestinal CSCs, existing approaches to define and isolate CSCs, and canonical molecular pathways involved in the regulation of gastrointestinal CSCs. More importantly, potential strategies targeting gastrointestinal CSCs are proposed to overcome the limitations of current therapies.

MedCommVol. 6(12)
University of Kentucky (US), Sichuan University (CN), Markey Cancer Center (US), Liaoning Cancer Hospital & Institute (CN), China Medical University (CN)
Openalex Percentile: Top 47%
Cancer Cells and Metastasis
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.