Title
Ispitivanje povezanosti imunohistohemijske ekspresije enzima popravke replikacionih grešaka DNK sa kliničkim i mikromorfološkim karakteristikama kolorektalnog karcinoma
Creator
Denčić, Tijana 1982-
Copyright date
2021
Object Links
Select license
Autorstvo-Nekomercijalno-Bez prerade 3.0 Srbija (CC BY-NC-ND 3.0)
License description
Dozvoljavate samo preuzimanje i distribuciju dela, ako/dok se pravilno naznačava ime autora, bez ikakvih promena dela i bez prava komercijalnog korišćenja dela. Ova licenca je najstroža CC licenca. Osnovni opis Licence: http://creativecommons.org/licenses/by-nc-nd/3.0/rs/deed.sr_LATN. Sadržaj ugovora u celini: http://creativecommons.org/licenses/by-nc-nd/3.0/rs/legalcode.sr-Latn
Language
Serbian
Cobiss-ID
Theses Type
Doktorska disertacija
description
Datum odbrane: 17.03.2021.
Other responsibilities
mentor
Krstić, Miljan 1973-
predsednik komisije
Jovičić Milentijević, Maja 1964-
član komisije
Petrović, Aleksandar 1970-
član komisije
Branković, Branko 1967-
član komisije
Šolajić, Nenad 1976-
Academic Expertise
Medicinske nauke
University
Univerzitet u Nišu
Faculty
Medicinski fakultet
Group
Katedra za patologiju
Alternative title
Immunohistochemical analysis of DNA mismatch repair deficiency in colorectal carcinoma and its association with clinical and micromorphological features
Publisher
[T. Denčić]
Format
[10], 117 listova
description
Biografija autora: list 117;
Bibliografija: 91-114.
description
Pathology
Abstract (en)
Deficient mismatch repair (MMR) status is associated with good
prognosis but poor therapeutic response to adjuvant chemotherapy in
patients with colorectal cancer. The study enrolled 104 patients
younger than 75 years of age with resected stage II and III colorectal
cancer samples from the period 2018–2019. All
immunohistochemistry analyses were done manually and performed
in the laboratories at the Department of Histology and Embryology,
Faculty of Medicine, University of Niš. The loss of nuclear
expression of at least one MMR protein was recorded in 12 (11.54%)
cases. The tumors with deficient and heterogeneity MMR status were
significantly associated with age up to 50 years and right-sided
localization. This prospective study of a single-center cohort of
patients with stage II and III colorectal cancer highlights the clinical
importance of using immunohistochemistry analysis as a guide for
diagnostic algorithm in a country with limited resources, but with a
high prevalence of colorectal carcinoma in the young patients. MMRdeficiency
tumors compared with proficient MMR colorectal cancer
was not shown to be a significant predictor of disease-free and overall
survival.
Authors Key words
Adjuvantna hemioterapija; Deficitarni MMR status; Kolorektalni
karcinom; Imunohistohemijska analiza
Authors Key words
Adjuvant chemotherapy; Deficient mismatch repair status; Colorectal
cancer; immunohistochemical analysis
Classification
616.348-006.6:577.175.213.3(043.3)
Subject
B-520
Type
Tekst
Abstract (en)
Deficient mismatch repair (MMR) status is associated with good
prognosis but poor therapeutic response to adjuvant chemotherapy in
patients with colorectal cancer. The study enrolled 104 patients
younger than 75 years of age with resected stage II and III colorectal
cancer samples from the period 2018–2019. All
immunohistochemistry analyses were done manually and performed
in the laboratories at the Department of Histology and Embryology,
Faculty of Medicine, University of Niš. The loss of nuclear
expression of at least one MMR protein was recorded in 12 (11.54%)
cases. The tumors with deficient and heterogeneity MMR status were
significantly associated with age up to 50 years and right-sided
localization. This prospective study of a single-center cohort of
patients with stage II and III colorectal cancer highlights the clinical
importance of using immunohistochemistry analysis as a guide for
diagnostic algorithm in a country with limited resources, but with a
high prevalence of colorectal carcinoma in the young patients. MMRdeficiency
tumors compared with proficient MMR colorectal cancer
was not shown to be a significant predictor of disease-free and overall
survival.
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