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dc.contributor.author Csermely, Péter
dc.contributor.author Korcsmáros T
dc.contributor.author Nussinov R
dc.date.accessioned 2022-06-30T12:24:49Z
dc.date.available 2022-06-30T12:24:49Z
dc.date.issued 2016
dc.identifier 84991108825
dc.identifier.citation pagination=55-59; journalVolume=58; journalTitle=SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/4914
dc.identifier.uri doi:10.1016/j.semcdb.2016.07.005
dc.description.abstract Cancer initiation and development are increasingly perceived as systems-level phenomena, where intra- and inter-cellular signaling networks of the ecosystem of cancer and stromal cells offer efficient methodologies for outcome prediction and intervention design. Within this framework, RAS emerges as a ‘contextual signaling hub’, i.e. the final result of RAS activation or inhibition is determined by the signaling network context. Current therapies often ‘train’ cancer cells shifting them to a novel attractor, which has increased metastatic potential and drug resistance. The few therapy-surviving cancer cells are surrounded by massive cell death triggering a primordial adaptive and reparative general wound healing response. Overall, dynamic analysis of patient- and disease-stage specific intracellular and intercellular signaling networks may open new areas of anticancer therapy using multitarget drugs, drugs combinations, edgetic drugs, as well as help design ‘gentler’, differentiation and maintenance therapies. © 2016 Elsevier Ltd
dc.relation.ispartof urn:issn:1084-9521
dc.title Intracellular and intercellular signaling networks in cancer initiation, development and precision anti-cancer therapy: RAS acts as contextual signaling hub
dc.type Journal Article
dc.date.updated 2018-02-20T13:24:36Z
dc.language.rfc3066 en
dc.identifier.mtmt 3135854


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