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dc.contributor.authorRungtawan Apinanen_US
dc.contributor.authorAnupong Makeudomen_US
dc.contributor.authorPaisan Kangvonkiten_US
dc.contributor.authorSangsom Prapayasatoken_US
dc.contributor.authorKajohnkiart Janebodinen_US
dc.contributor.authorChayarop Supancharten_US
dc.contributor.authorDumnoensun Pruksakornen_US
dc.contributor.authorSuttichai Krisanaprakornkiten_US
dc.date.accessioned2022-05-27T08:36:05Z-
dc.date.available2022-05-27T08:36:05Z-
dc.date.issued2022-03-01en_US
dc.identifier.issn01252208en_US
dc.identifier.other2-s2.0-85127130406en_US
dc.identifier.other10.35755/jmedassocthai.2022.03.13281en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85127130406&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/73136-
dc.description.abstractObjective: Salivary glands are frequently exposed to X-radiation during dental radiography. The present study aimed to investigate the proliferative and apoptotic effects of low-dose irradiation on human salivary cell lines in vitro. Materials and Methods: Two distinct ductal cell lines, HSG and HSY, were first characterized by expressions of carcinoembryonic antigen (CEA) and lactoferrin (LF), compared to those in human oral keratinocytes (HOKs), and then examined for their doubling times. They were exposed to periapical radiography for 5, 10, or 20 times, and incubated further for 1, 3, or 5 cycles of their cell division. Cell proliferation was examined by a BrdU assay and immunoblot analysis of Ki-67 expression. Cell apoptosis was determined by the presence of human active caspase 3. Results: The mean degrees of CEA and LF expressions were significantly higher in HSG and HSY than in HOKs (p<0.01). The doubling time of HSG was significantly shorter than that of HSY (p=0.009). Upon repeated exposures to dental X-ray, the proliferation of HSG was significantly increased at the first cycle, whereas that of HSY was significantly decreased (p<0.05). At the third cycle, Ki-67 expression was significantly increased in HSG, while it was significantly decreased in HSY (p=0.037). However, the proliferative effect was temporarily presented in both cells. No active caspase 3 was detected upon exposure to any doses or in any cycles. Conclusion: The two ductal cell lines demonstrated adaptive response to low-dose irradiation by either increased or decreased cell proliferation, but no apoptosis was found in both cell lines.en_US
dc.subjectMedicineen_US
dc.titleDifferential Proliferative Responses to Low-Dose Irradiation between Human Submandibular and Parotid Salivary Ductal Cell Linesen_US
dc.typeJournalen_US
article.title.sourcetitleJournal of the Medical Association of Thailanden_US
article.volume105en_US
article.stream.affiliationsMahidol University, Faculty of Dentistryen_US
article.stream.affiliationsFaculty of Medicine, Chiang Mai Universityen_US
article.stream.affiliationsMae Fah Luang Universityen_US
article.stream.affiliationsChiang Mai Universityen_US
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