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Bacterial, Archaea, and Viral Transcripts (BAVT) Expression in Gynecological Cancers and Correlation with Regulatory Regions of the Genome
Review

Histopathologic, Genetic and Molecular Characterization of Endometrial Cancer Racial Disparity

1
Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, Stephenson Cancer Center, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA
2
Arkansas College of Osteopathic Medicine, Fort Smith, AR 72916, USA
*
Authors to whom correspondence should be addressed.
Academic Editor: Ruud L. M. Bekkers
Cancers 2021, 13(8), 1900; https://doi.org/10.3390/cancers13081900
Received: 30 January 2021 / Revised: 30 March 2021 / Accepted: 12 April 2021 / Published: 15 April 2021
Black patients are diagnosed and die earlier of endometrial cancer in comparison with their White counterparts. Factors that have been implicated in this racial disparity, such as socioeconomic status, increased frequencies of more aggressive tumor histology, and comorbid conditions, do not account for all of the disparity. Molecular defects in the endometrial tumors likely also contribute to the more aggressive tumor biology and the patient disparities. In this study, we reviewed the published data of molecular characteristics of endometrial cancer in different races. The majority of the publications compare Black and White patients, and identify molecules and pathways that can be targeted with existing drugs. These findings encourage molecular profile studies comparing additional races and ethnicities, and development of race-specific treatments.
In contrast to the decline in incidence and mortality of most other cancers, these rates are rising for endometrial cancer. Black women with endometrial cancer have earlier diagnosis, more aggressive histology, advanced stage and worse outcomes compared with their White counterparts. Socioeconomic status, a higher incidence of aggressive histology, and comorbid conditions are known factors leading to racial disparity in patients with endometrial cancer; nevertheless, they do not account for the entire racial disparity; which emphasizes the roles of molecular, histopathological and genetic factors. We performed a comprehensive review of all published scientific literature up to January 2021 reporting histopathologic, genetic and molecular factors associated with racial disparities in patients with endometrial cancer. The interactions and pathways of molecules reported to have significant differential expression in endometrial cancers from Black and White patients were identified with Ingenuity Pathway Analysis. The majority of studies compared Black and White patients; however, limited data are available for other racial and ethnic groups. Reported differences that could account for the worse survival of Black endometrial cancer patients include more aggressive histopathologies and molecular alterations, including upregulation of molecules driving cell cycle progression, and p53 and HER2/NEU signaling. Several of these molecules are targeted by existing pharmaceuticals. These findings encourage further study and the development of race-specific treatment strategies. View Full-Text
Keywords: endometrial cancer; racial disparity; histopathology; molecular profile; targeted agents endometrial cancer; racial disparity; histopathology; molecular profile; targeted agents
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MDPI and ACS Style

Javadian, P.; Washington, C.; Mukasa, S.; Benbrook, D.M. Histopathologic, Genetic and Molecular Characterization of Endometrial Cancer Racial Disparity. Cancers 2021, 13, 1900. https://doi.org/10.3390/cancers13081900

AMA Style

Javadian P, Washington C, Mukasa S, Benbrook DM. Histopathologic, Genetic and Molecular Characterization of Endometrial Cancer Racial Disparity. Cancers. 2021; 13(8):1900. https://doi.org/10.3390/cancers13081900

Chicago/Turabian Style

Javadian, Pouya, Christina Washington, Shylet Mukasa, and Doris M. Benbrook. 2021. "Histopathologic, Genetic and Molecular Characterization of Endometrial Cancer Racial Disparity" Cancers 13, no. 8: 1900. https://doi.org/10.3390/cancers13081900

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