Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/106738
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dc.contributor.authorMarques, M. P. M.-
dc.contributor.authorBatista de Carvalho, A. L. M.-
dc.contributor.authorMamede, A. P.-
dc.contributor.authorDopplapudi, A.-
dc.contributor.authorGarcía Sakai, V.-
dc.contributor.authorBatista de Carvalho, L. A. E.-
dc.date.accessioned2023-04-20T09:39:47Z-
dc.date.available2023-04-20T09:39:47Z-
dc.date.issued2020-09-
dc.identifier.issn2329-7778-
dc.identifier.urihttps://hdl.handle.net/10316/106738-
dc.description.abstractThe transition from normal to malignant state in human cells is still a poorly understood process. Changes in the dynamical activity of intracellular water between healthy and cancerous human cells were probed as an innovative approach for unveiling particular features of malignancy and identifying specific reporters of cancer. Androgen-unresponsive prostate and triple-negative breast carcinomas were studied as well as osteosarcoma, using the technique of quasi-elastic neutron scattering. The cancerous cells showed a considerably higher plasticity relative to their healthy counterparts, this being more significant for the mammary adenocarcinoma. Also, the data evidence that the prostate cancer cells display the highest plasticity when compared to triple-negative mammary cancer and osteosarcoma, the latter being remarkably less flexible. Furthermore, the results suggest differences between the flexibility of different types of intracellular water molecules in normal and cancerous cells, as well as the number of molecules involved in the different modes of motion. The dynamics of hydration water molecules remain virtually unaffected when going from healthy to cancer cells, while cytoplasmic water (particularly the rotational motions) undergoes significant changes upon normal-to-cancer transition. The results obtained along this study can potentially help to understand the variations in cellular dynamics underlying carcinogenesis and tumor metastasis, with an emphasis on intracellular water.pt
dc.language.isoengpt
dc.publisherAAPM - American Association of Physicists in Medicinept
dc.relationThis work was supported by POCentro, COMPETE 2020, Portugal 2020, and European Community through the FEDER and by the Portuguese Foundation for Science and Technology (Nos. Centro-01–0145-FEDER-029956 and UIDB/00070/2020). The STFC Rutherford Appleton Laboratory is thanked for access to the neutron beam facilities (No. OSIRIS/RB1910015, DOI: 10.5286/ ISIS.E.RB1910015). We also acknowledge the support of the National Institute of Standards and Technology, U.S. Department of Commerce, in providing the neutron research facilities used in this work—access to HFBS (B38–16) was provided by the Centre for High Resolution Neutron Scattering, a partnership between the National Institute of Standards and Technology and the National Science Foundation under Agreement No. DMR-1508249.pt
dc.rightsopenAccesspt
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt
dc.titleRole of intracellular water in the normal-to-cancer transition in human cells-insights from quasi-elastic neutron scatteringpt
dc.typearticlept
degois.publication.firstPage054701pt
degois.publication.issue5pt
degois.publication.titleStructural Dynamicspt
dc.peerreviewedyespt
dc.identifier.doi10.1063/4.0000021-
degois.publication.volume7pt
dc.date.embargo2020-09-01*
dc.identifier.pmid32923512-
uc.date.periodoEmbargo0pt
item.grantfulltextopen-
item.cerifentitytypePublications-
item.languageiso639-1en-
item.openairetypearticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextCom Texto completo-
crisitem.author.researchunitQFM-UC – Molecular Physical-Chemistry R&D Unit-
crisitem.author.orcid0000-0002-8391-0055-
crisitem.author.orcid0000-0002-0647-4771-
Appears in Collections:I&D QFM-UC - Artigos em Revistas Internacionais
FCTUC Ciências da Vida - Artigos em Revistas Internacionais
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