Cancer stem cells in human gastrointestinal cancer

被引:65
作者
Taniguchi, Hiroaki [1 ]
Moriya, Chiharu [1 ]
Igarashi, Hisayoshi [1 ]
Saitoh, Anri [1 ]
Yamamoto, Hiroyuki [2 ]
Adachi, Yasushi [3 ]
Imai, Kohzoh [4 ]
机构
[1] Univ Tokyo, Inst Med Sci, Res Hosp, Ctr Antibody & Vaccine Therapy, Tokyo, Japan
[2] St Marianna Univ, Sch Med, Dept Internal Med, Div Gastroenterol & Hepatol, Kawasaki, Kanagawa, Japan
[3] Sapporo Med Univ, Sch Med, Dept Gastroenterol Rheumatol & Clin Immunol, Sapporo, Hokkaido, Japan
[4] Univ Tokyo, Inst Med Sci, Tokyo, Japan
关键词
Cancer stem cell; drug resistance; gastrointestinal cancer; neoplasm metastasis; phenotype of cancer stem cell; TUMOR-INITIATING CELLS; SELF-RENEWAL; LIVER; IDENTIFICATION; CARCINOMA; PROMOTES; MARKER; COLON; EPCAM; INVASION;
D O I
10.1111/cas.13069
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cancer stem cells (CSCs) are thought to be responsible for tumor initiation, drug and radiation resistance, invasive growth, metastasis, and tumor relapse, which are the main causes of cancer-related deaths. Gastrointestinal cancers are the most common malignancies and still the most frequent cause of cancer-related mortality worldwide. Because gastrointestinal CSCs are also thought to be resistant to conventional therapies, an effective and novel cancer treatment is imperative. The first reported CSCs in a gastrointestinal tumor were found in colorectal cancer in 2007. Subsequently, CSCs were reported in other gastrointestinal cancers, such as esophagus, stomach, liver, and pancreas. Specific phenotypes could be used to distinguish CSCs from non-CSCs. For example, gastrointestinal CSCs express unique surface markers, exist in a side-population fraction, show high aldehyde dehydrogenase-1 activity, form tumorspheres when cultured in non-adherent conditions, and demonstrate high tumorigenic potential in immunocompromised mice. The signal transduction pathways in gastrointestinal CSCs are similar to those involved in normal embryonic development. Moreover, CSCs are modified by the aberrant expression of several microRNAs. Thus, it is very difficult to target gastrointestinal CSCs. This review focuses on the current research on gastrointestinal CSCs and future strategies to abolish the gastrointestinal CSC phenotype.
引用
收藏
页码:1556 / 1562
页数:7
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