MARINOVIC, S., A. SKRTIC, Tina CATELA IVKOVIĆ, M. POLJAK a S. KAPITANOVIC. Regulation of KRAS protein expression by miR-544a and KRAS-LCS6 polymorphism in wild-type KRAS sporadic colon adenocarcinoma. HUMAN CELL. TOKYO: SPRINGER JAPAN KK, 2021, roč. 34, č. 5, s. 1455-1465. ISSN 0914-7470. Dostupné z: https://dx.doi.org/10.1007/s13577-021-00576-2.
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Základní údaje
Originální název Regulation of KRAS protein expression by miR-544a and KRAS-LCS6 polymorphism in wild-type KRAS sporadic colon adenocarcinoma
Autoři MARINOVIC, S., A. SKRTIC, Tina CATELA IVKOVIĆ (191 Chorvatsko, garant, domácí), M. POLJAK a S. KAPITANOVIC.
Vydání HUMAN CELL, TOKYO, SPRINGER JAPAN KK, 2021, 0914-7470.
Další údaje
Originální jazyk angličtina
Typ výsledku Článek v odborném periodiku
Obor 10601 Cell biology
Stát vydavatele Japonsko
Utajení není předmětem státního či obchodního tajemství
WWW URL
Impakt faktor Impact factor: 4.374
Kód RIV RIV/00216224:14740/21:00124258
Organizační jednotka Středoevropský technologický institut
Doi http://dx.doi.org/10.1007/s13577-021-00576-2
UT WoS 000671907000001
Klíčová slova anglicky Colon adenocarcinoma; Immunohistochemistry; KRAS; Let-7a; miR-544a
Štítky rivok
Příznaky Mezinárodní význam, Recenzováno
Změnil Změnila: Mgr. Pavla Foltynová, Ph.D., učo 106624. Změněno: 22. 2. 2022 18:08.
Anotace
Colorectal carcinoma (CRC) results from the accumulation of genetic mutations and alterations in signaling pathways. KRAS is mutated in 40% of CRC cases and is involved in increased tumor cells proliferation and survival. Although KRAS mutations are a dominant event in CRC tumorigenesis, increased wild-type KRAS expression has a similar effect on accelerated tumor growth. In this study, we investigated the KRAS status in correlation with clinicopathological features in sporadic CRC and more importantly the role of let-7a-5p and miR-544a-3p in the regulation of wild-type KRAS protein expression in the tumor center (T1) and invasive tumor front (T2). Analysis showed that 39.1% of tumor samples had KRAS mutations. In wild-type KRAS tumors, 62.0% were positive for KRAS protein expression and there was a higher percentage of KRAS-positive tumor cells and a higher intensity of immunohistochemical reaction in T2 than in T1 samples. This could not be attributed to differences in KRAS mRNA levels, suggesting regulation via miR-544a-3p expression which was significantly decreased in T2 samples. Furthermore, we demonstrated that tumor samples carrying the KRAS-LCS6 variant allele had significantly higher protein expression of the wild-type KRAS. Our results suggest the role of the KRAS-LCS6 polymorphism and miR-544a-3p expression in the regulation of wild-type KRAS protein expression in sporadic CRC.
VytisknoutZobrazeno: 2. 9. 2024 06:39