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Immunohistochemical Expression of Fn14 and Cath-D as Prognostic Biological Markers and Compare with Histological Reaction in Invasive Human Breast Cancer

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dc.contributor.author Sabah, Ali Mugahed Al-Qadasi
dc.contributor.author Saeed, Mahmoud Saeed Mohamed
dc.contributor.author Roa, Mohmed Mahmoud Sultan
dc.date.accessioned 2023-01-04T10:36:32Z
dc.date.available 2023-01-04T10:36:32Z
dc.date.issued 2023-01-04
dc.identifier.uri http://dspacewku.repository.edu.sd/handle/123456789/2949
dc.description Scholars Journal of Applied Medical Sciences en_US
dc.description.abstract Fibroblast growth factor-inducible-14 (Fn14) is a 14-kDa type I transmembrane receptor located on chromosome 16p13. Fn14 is a member of the tumor necrosis factor receptor super family that normally expressed in healthy tissues, but its expression is increased in injured tissue where it thought to play role in tissue remodeling. Cathepsin D (Cath D) is a soluble lysosomal aspartyl glycoprotease that can degrade the protein components of the matrix and free growth factors therein embedded, thus favoring tumor growth, invasion and angiogenesis. The aim of the present work was to investigate the expression of Fn14 and Cathepsin D as novel prognostic biomarkers in human invasive ductal carcinoma (IDC) versus benign tumors and normal breast tissues as well as their correlation with different pathological and histological parameters. Immunohistochemical technique was used to examine the expression of Fn14 and Cath-D in normal, benign as well as in IDC. Present results showed higher expression of Fn14 and Cath-D in IDC comparing to normal and benign breast tissues. Keywords: Fn14 and Cathepsin D prognostic marker en_US
dc.description.sponsorship جامعة غرب كردفان en_US
dc.language.iso other en_US
dc.publisher جامعة غرب كردفان en_US
dc.subject distribution en_US
dc.subject which permits unrestricted use, en_US
dc.subject author and source are credited en_US
dc.title Immunohistochemical Expression of Fn14 and Cath-D as Prognostic Biological Markers and Compare with Histological Reaction in Invasive Human Breast Cancer en_US
dc.type Other en_US


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