Novel Paired Normal Prostate and Prostate Cancer Model Cell Systems Derived from African American Patients.


Journal

Cancer research communications
ISSN: 2767-9764
Titre abrégé: Cancer Res Commun
Pays: United States
ID NLM: 9918281580506676

Informations de publication

Date de publication:
12 2022
Historique:
received: 19 05 2022
revised: 27 07 2022
accepted: 30 11 2022
entrez: 27 3 2023
pubmed: 28 3 2023
medline: 28 3 2023
Statut: epublish

Résumé

Prostate cancer is the most frequently diagnosed solid malignancy in men. African American (AA) men are at greater risk for developing prostate cancer, and experience higher mortality rates, as compared with Caucasian American men. However, mechanistic studies to understand this health disparity have been limited by the lack of relevant Cells derived from prostatectomies of AA patients conferred a bimodal cellular phenotype, recapitulating clinical prostate cellular complexity in this model cell system. Comparisons of viability responses of tumor derived to normal epithelial cells offer the potential for screening therapeutic drugs. Therefore, these paired prostate epithelial cell cultures provide an

Identifiants

pubmed: 36970725
doi: 10.1158/2767-9764.CRC-22-0203
pii: CRC-22-0203
pmc: PMC10035501
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Pagination

1617-1625

Subventions

Organisme : NCI NIH HHS
ID : HHSN261201800016C
Pays : United States

Informations de copyright

© 2022 The Authors; Published by the American Association for Cancer Research.

Déclaration de conflit d'intérêts

M. Jung reports other from Shuttle Pharmaceuticals, Inc outside the submitted work. S. Grindrod reports grants from Shuttle Pharmaceuticals Inc during the conduct of the study; grants from Shuttle Pharmaceuticals Inc outside the submitted work. A. Dritschilo reports grants from NIH SBIR during the conduct of the study; other from Shuttle Pharmaceuticals, Inc. outside the submitted work. No disclosures were reported by the other authors.

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Auteurs

Mira Jung (M)

Department of Radiation Medicine, Georgetown University School of Medicine, Washington, District of Columbia.

Keith Kowalczyk (K)

Department of Urology, Georgetown University School of Medicine, Washington, District of Columbia.
MedStar Georgetown University Hospital, Washington, District of Columbia.

Ryan Hankins (R)

Department of Urology, Georgetown University School of Medicine, Washington, District of Columbia.
MedStar Georgetown University Hospital, Washington, District of Columbia.

Gaurav Bandi (G)

Department of Urology, Georgetown University School of Medicine, Washington, District of Columbia.
MedStar Georgetown University Hospital, Washington, District of Columbia.

Bhaskar Kallakury (B)

Department of Pathology, Georgetown University School of Medicine, Washington, District of Columbia.
MedStar Georgetown University Hospital, Washington, District of Columbia.

Michael A Carrasquilla (MA)

Department of Radiation Medicine, Georgetown University School of Medicine, Washington, District of Columbia.
MedStar Georgetown University Hospital, Washington, District of Columbia.

Partha P Banerjee (PP)

Department of Biochemistry and Molecular & Cellular Biology, Georgetown University School of Medicine, Washington, District of Columbia.

Scott Grindrod (S)

Shuttle Pharmaceuticals, Inc, Rockville, Maryland.

Anatoly Dritschilo (A)

Department of Radiation Medicine, Georgetown University School of Medicine, Washington, District of Columbia.
MedStar Georgetown University Hospital, Washington, District of Columbia.
Shuttle Pharmaceuticals, Inc, Rockville, Maryland.

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