Abstract

Accumulating evidence has shown that cancer stem cells (CSCs) have a tumour-initiating capacity and play crucial roles in tumour metastasis, relapse and chemo/radio-resistance. As tumour propagation initiators, CSCs are considered to be promising targets for obtaining a better therapeutic outcome. Cervical carcinoma is the most common gynaecological malignancy and has a high cancer mortality rate among females. As a result, the investigation of cervical cancer stem cells (CCSCs) is of great value. However, the numbers of cancer cells and corresponding CSCs in malignancy are dynamically balanced, and CSCs may reside in the CSC niche, about which little is known to date. Therefore, due to their complicated molecular phenotypes and biological behaviours, it remains challenging to obtain “purified” CSCs and continuously culture CSCs for further in vitro studies without the cells losing their stem properties. At present, CSC-related markers and functional assays are used to purify, identify and therapeutically target CSCs both in vitro and in vivo. Nevertheless, CSC-related markers are not universal to all tumour types, although some markers may be valid in multiple tumour types. Additionally, functional identifications based on CSC-specific properties are usually limited in in vivo studies. Furthermore, an optimal method for identifying potential CCSCs in CCSC studies has not been previously published, and these techniques are currently of great importance. This article updates our knowledge on CSCs and CCSCs, reviews potential stem cell markers and functional assays for identifying CCSCs, and describes the potential of targeting CCSCs in the treatment of cervical carcinoma.

Highlights

  • Cancer stem cells (CSCs) are believed to be a small subpopulation of tumour cells that have properties of tumorigenesis, multilineage differentiation potential, selfrenewal [1], slow cycling capacity [2] and tumorigenicity [3, 4]

  • Circulating tumour cells (CTCs), which are present in the blood, and disseminated tumour cells (DTCs), which are located in a secondary organ, are positively associated with tumour metastasis, relapse and poor survival [29,30,31,32,33]

  • We reviewed and summarized the markers for cancer stem cells (CCSCs) that are currently used or are potential candidates in CCSC studies (Table 1)

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Summary

Introduction

Cancer stem cells (CSCs) are believed to be a small subpopulation of tumour cells that have properties of tumorigenesis, multilineage differentiation potential, selfrenewal [1], slow cycling capacity [2] and tumorigenicity [3, 4]. Self-renewal, chemo/ radio-resistance, limiting dilution tumorigenicity, multilineage differentiation, anti-apoptosis, highly expressing OCT4, ABCG2, SOX2 [98,99,100] SOX2 overin cervical carcinoma expressing cells by Differentiation, self-renewal, enhanced than normal cervix plasmid transfection tumorigenicity, highly expressing stem cell [129,130,131], in high grade and cell sorting by markers OCT4, ALDH1, BMI1 and EMT-related of dysplasia than low

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