NARA Discovery
Article Details
← Back to Search Results
Journal Article

Clusterin: a marker and mediator of chemoresistance in colorectal cancer

Sara Hlavca; Wing Hei Chan; Rebekah M. Engel; Helen E. Abud
Cancer and Metastasis Reviews · Vol. 43, Issue 1 · pp. 379-391 · 2024

Abstract

Intra-tumoural heterogeneity and cancer cell plasticity in colorectal cancer (CRC) have been key challenges to effective treatment for patients. It has been suggested that a subpopulation of LGR5-expressing cancer stem cells (CSCs) is responsible for driving tumour relapse and therapy resistance in CRC. However, studies have revealed that the LGR5 +ve CSC population is highly sensitive to chemotherapy. It has been hypothesised that another subset of tumour cells can phenotypically revert to a stem-like state in response to chemotherapy treatment which replenishes the LGR5 +ve CSC population and maintains tumour growth. Recently, a unique stem cell population marked by enriched clusterin (CLU) expression and termed the revival stem cell (RevSC) was identified in the regenerating murine intestine. This CLU-expressing cell population is quiescent during homeostasis but has the ability to survive and regenerate other stem cells upon injury. More recently, the CLU +ve signature has been implicated in several adverse outcomes in CRC, including chemotherapy resistance and poor patient survival; however, the mechanism behind this remains undetermined. In this review, we discuss recent insights on CLU in CRC and its roles in enhancing the plasticity of cells and further consider the implications of CLU as a prospective target for therapeutic intervention.

Bibliographic Information

JournalCancer and Metastasis Reviews
PublisherSpringer
Publication Date2024-03-01
Publication Year2024
Volume43
Issue1
Pages379-391
Document TypeJournal Article
eISSN1573-7233
DOI10.1007/s10555-024-10173-y

Access Information

NARA Access Coverage1982-01-01~Current
Journal Homepagehttps://www.springer.com/journal/10555
Publisher PageOpen Publisher Page
Full-text access depends on NARA's subscribed coverage and institutional access.