» Articles » PMID: 35806410

PAX8 in the Junction Between Development and Tumorigenesis

Overview
Journal Int J Mol Sci
Publisher MDPI
Date 2022 Jul 9
PMID 35806410
Authors
Affiliations
Soon will be listed here.
Abstract

Normal processes of embryonic development and abnormal transformation to cancer have many parallels, and in fact many aberrant cancer cell capabilities are embryonic traits restored in a distorted, unorganized way. Some of these capabilities are cell autonomous, such as proliferation and resisting apoptosis, while others involve a complex interplay with other cells that drives significant changes in neighboring cells. The correlation between embryonic development and cancer is driven by shared proteins. Some embryonic proteins disappear after embryogenesis in adult differentiated cells and are restored in cancer, while others are retained in adult cells, acquiring new functions upon transformation to cancer. Many embryonic factors embraced by cancer cells are transcription factors; some are master regulators that play a major role in determining cell fate. The paired box (PAX) domain family of developmental transcription factors includes nine members involved in differentiation of various organs. All paired box domain proteins are involved in different cancer types carrying pro-tumorigenic or anti-tumorigenic roles. This review focuses on PAX8, a master regulator of transcription in embryonic development of the thyroid, kidney, and male and female genital tracts. We detail the role of PAX8 in each of these organ systems, describe its role during development and in the adult if known, and highlight its pro-tumorigenic role in cancers that emerge from PAX8 expressing organs.

Citing Articles

Current advances in understanding endometrial epithelial cell biology and therapeutic applications for intrauterine adhesion.

Wang J, Zhan H, Wang Y, Zhao L, Huang Y, Wu R Stem Cell Res Ther. 2024; 15(1):379.

PMID: 39456113 PMC: 11515228. DOI: 10.1186/s13287-024-03989-6.


METTL3 regulates thyroid cancer differentiation and chemosensitivity by modulating PAX8.

Kang N, Zhao Z, Wang Z, Ning J, Wang H, Zhang W Int J Biol Sci. 2024; 20(9):3426-3441.

PMID: 38993572 PMC: 11234206. DOI: 10.7150/ijbs.84797.


The Role of the PAX Genes in Renal Cell Carcinoma.

Li L, Hossain S, Eccles M Int J Mol Sci. 2024; 25(12).

PMID: 38928435 PMC: 11203709. DOI: 10.3390/ijms25126730.


Prognostic value of PAX8 in small cell lung cancer.

Tao F, Zhu H, Xu J, Guo Y, Wang X, Shao L Heliyon. 2024; 10(7):e28251.

PMID: 38596099 PMC: 11002052. DOI: 10.1016/j.heliyon.2024.e28251.


In Silico Functional and Structural Analysis of Non-synonymous Single Nucleotide Polymorphisms (nsSNPs) in Human Paired Box 4 Gene.

Kamal M, Islam M, Rabby M, Zahid M, Hasan M Biochem Genet. 2023; 62(4):2975-2998.

PMID: 38062275 DOI: 10.1007/s10528-023-10589-1.

References
1.
Grote D, Souabni A, Busslinger M, Bouchard M . Pax 2/8-regulated Gata 3 expression is necessary for morphogenesis and guidance of the nephric duct in the developing kidney. Development. 2005; 133(1):53-61. DOI: 10.1242/dev.02184. View

2.
Rodgers L, O hAinmhire E, Young A, Burdette J . Loss of PAX8 in high-grade serous ovarian cancer reduces cell survival despite unique modes of action in the fallopian tube and ovarian surface epithelium. Oncotarget. 2016; 7(22):32785-95. PMC: 5078051. DOI: 10.18632/oncotarget.9051. View

3.
Orvis G, Behringer R . Cellular mechanisms of Müllerian duct formation in the mouse. Dev Biol. 2007; 306(2):493-504. PMC: 2730733. DOI: 10.1016/j.ydbio.2007.03.027. View

4.
Fares B, Berger L, Bangiev-Girsh E, Kakun R, Ghannam-Shahbari D, Tabach Y . PAX8 plays an essential antiapoptotic role in uterine serous papillary cancer. Oncogene. 2021; 40(34):5275-5285. DOI: 10.1038/s41388-021-01925-z. View

5.
Tai T, Jennermann C, Brown K, OLIVER B, MacGinnitie M, Wilkison W . Activation of the nuclear receptor peroxisome proliferator-activated receptor gamma promotes brown adipocyte differentiation. J Biol Chem. 1996; 271(47):29909-14. DOI: 10.1074/jbc.271.47.29909. View