Abstract

MicroRNAs (miRNAs) have a critical role in regulating stem cells (SCs) during development, and because aberrant expression of miRNAs occurs in various cancers, our goal was to determine if dysregulation of miRNAs is involved in the SC origin of colorectal cancer (CRC). We previously reported that aldehyde dehydrogenase (ALDH) is a marker for normal and malignant human colonic SCs and tracks SC overpopulation during colon tumorigenesis. MicroRNA expression was studied in ALDH-positive SCs from normal and malignant human colon tissues by Nanostring miRNA profiling. Our findings show that: (1) A unique miRNA signature distinguishes ALDH-positive CRC cells from ALDH-positive normal colonic epithelial cells, (2) Expression of four miRNAs (miRNA200c, miRNA92a, miRNA20a, miRNA93) are significantly altered in CRC SCs compared to normal colonic SCs, (3) miRNA92a expression is also upregulated in ALDH-positive HT29 CRC SCs as compared to ALDH-negative SCs, (4) miRNA92a targets the 3′UTR of LRIG1 SC gene, and (5) miRNA92a modulates proliferation of HT29 CRC cells. Thus, our findings indicate that overexpression of miRNA92a contributes to the SC origin of CRC. Strategies designed to modulate miRNA expression, such as miRNA92a, may provide ways to target malignant SCs and to develop more effective therapies against CRC.

Highlights

  • A significant body of scientific evidence indicates that: (i) stem cells (SCs) are the cells of origin of cancer [1,2], (ii) SC overpopulation drives tumor initiation and progression [3,4,5], (iii) SCs are resistant to conventional anti-cancer therapies

  • Fluorescence microscopy analysis showed that cells at the bottom of normal colonic crypts display intense green fluorescence signal indicating that cells in the crypt SC niche have high aldehyde dehydrogenase (ALDH) activity (Figure 1A,B)

  • Fluorescence microscopic analysis of dissociated cells derived from both fresh normal crypts and colorectal cancer (CRC) tissues showed that these colonic tissues contain specific subpopulations of ALDEFLUOR-positive cells (Figure 1C)

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Summary

Introduction

A significant body of scientific evidence indicates that: (i) stem cells (SCs) are the cells of origin of cancer [1,2], (ii) SC overpopulation drives tumor initiation and progression [3,4,5], (iii) SCs are resistant to conventional anti-cancer therapies. While our findings on ALDH and many results on various SC markers by others indicates that cancer SC (CSC) overpopulation drives tumor growth, it is not fully understood which dysregulated mechanisms cause the SC overpopulation. Because evidence indicates miRNAs have an important role in the pathogenesis of various cancers, we have been studying changes in miRNAs as a possible mechanism in colorectal cancer (CRC). Mounting evidence indicates a role for miRNAs in the maintenance of the CSC phenotype [12,13,14,15,16]. We have been focusing on miRNAs that contribute to maintenance of the phenotype of colonic CSCs

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