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Review
. 2022 Feb 16:13:823572.
doi: 10.3389/fphar.2022.823572. eCollection 2022.

Gynecologic Cancer, Cancer Stem Cells, and Possible Targeted Therapies

Affiliations
Review

Gynecologic Cancer, Cancer Stem Cells, and Possible Targeted Therapies

Vahideh Keyvani et al. Front Pharmacol. .

Abstract

Gynecologic cancer is one of the main causes of death in women. In this type of cancer, several molecules (oncogenes or tumor suppressor genes) contribute to the tumorigenic process, invasion, metastasis, and resistance to treatment. Based on recent evidence, the detection of molecular changes in these genes could have clinical importance for the early detection and evaluation of tumor grade, as well as the selection of targeted treatment. Researchers have recently focused on cancer stem cells (CSCs) in the treatment of gynecologic cancer because of their ability to induce progression and recurrence of malignancy. This has highlighted the importance of a better understanding of the molecular basis of CSCs. The purpose of this review is to focus on the molecular mechanism of gynecologic cancer and the role of CSCs to discover more specific therapeutic approaches to gynecologic cancer treatment.

Keywords: cancer stem cells; carcinogenesis; cervical cancer; chemoresistance; endometrial cancer; gynecologic cancer; molecular mechanism; ovarian cancer.

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Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

FIGURE 1
FIGURE 1
Different factors and signaling pathways mediating stem cell self-renewal, differentiation, and metastasis. (The figure was reprinted from Zuber et al.’s (2020) study.)
FIGURE 2
FIGURE 2
Effectiveness of targeted CSC therapy in combination with conventional chemotherapy. Conventional chemotherapy can decrease tumor size by acting on non-CSC tumor cells; however, tumor recurrence associated with CSCs may lead to treatment failure. Targeting the CSCs could reduce numbers of CSCs followed by better response of tumors to therapy. (The figure was reprinted from Kyo’s (2013) study.)

References

    1. Ahmed N., Abubaker K., Findlay J., Quinn M. (2010). Epithelial Mesenchymal Transition and Cancer Stem Cell-like Phenotypes Facilitate Chemoresistance in Recurrent Ovarian Cancer. Curr. Cancer Drug Targets 10 (3), 268–278. 10.2174/156800910791190175 - DOI - PubMed
    1. Ahn M. Y., Jung J. H., Na Y. J., Kim H. S. (2008). A Natural Histone Deacetylase Inhibitor, Psammaplin A, Induces Cell Cycle Arrest and Apoptosis in Human Endometrial Cancer Cells. Gynecol. Oncol. 108 (1), 27–33. 10.1016/j.ygyno.2007.08.098 - DOI - PubMed
    1. Amant F., Moerman P., Neven P., Timmerman D., Van Limbergen E., Vergote I. (2005). Endometrial Cancer. Lancet 366 (9484), 491–505. 10.1016/S0140-6736(05)67063-8 - DOI - PubMed
    1. Androutsopoulos G., Michail G., Adonakis G., Decavalas G. (2015). Current Treatment Approach of Endometrial Cancer. Int. J. Clin. Ther. Diagn. 1 (3), 8–11. 10.19070/2332-2926-SI01003 - DOI
    1. Antoniou A., Pharoah P. D., Narod S., Risch H. A., Eyfjord J. E., Hopper J. L., et al. (2003). Average Risks of Breast and Ovarian Cancer Associated with BRCA1 or BRCA2 Mutations Detected in Case Series Unselected for Family History: a Combined Analysis of 22 Studies. Am. J. Hum. Genet. 72 (5), 1117–1130. 10.1086/375033 - DOI - PMC - PubMed

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