A prototypical non-malignant epithelial model to study genome dynamics and concurrently monitor micro-RNAs and proteins in situ during oncogene-induced senescence.
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Authors
Komseli, EPateras, I
Krejsgaard, T
Stawiski, K
Rizou, S
Polyzos, A
Roumelioti, F
Chiourea, M
Mourkioti, I
Paparouna, E
Zampetidis, C
Gumeni, S
Trougakos, I
Pefani, D
O'Neill, E
Gagos, S
Eliopoulos, A
Fendler, W
Chowdhury, D
Bartek, J
Gorgoulis, Vassilis G
Affiliation
Molecular Carcinogenesis Group, Department of Histology and Embryology, School of Medicine, National & Kapodistrian University of Athens, 75 Mikras Asias St, GR-11527, Athens, GreeceIssue Date
2018-01-10
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Senescence is a fundamental biological process implicated in various pathologies, including cancer. Regarding carcinogenesis, senescence signifies, at least in its initial phases, an anti-tumor response that needs to be circumvented for cancer to progress. Micro-RNAs, a subclass of regulatory, non-coding RNAs, participate in senescence regulation. At the subcellular level micro-RNAs, similar to proteins, have been shown to traffic between organelles influencing cellular behavior. The differential function of micro-RNAs relative to their subcellular localization and their role in senescence biology raises concurrent in situ analysis of coding and non-coding gene products in senescent cells as a necessity. However, technical challenges have rendered in situ co-detection unfeasible until now.Citation
A prototypical non-malignant epithelial model to study genome dynamics and concurrently monitor micro-RNAs and proteins in situ during oncogene-induced senescence. 2018, 19 (1):37 BMC GenomicsJournal
BMC GenomicsDOI
10.1186/s12864-017-4375-1PubMed ID
29321003Type
ArticleLanguage
enISSN
1471-2164ae974a485f413a2113503eed53cd6c53
10.1186/s12864-017-4375-1
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