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dc.contributor.authorCheng, Hao-Yuanen_US
dc.contributor.authorKo, Fu-Hsiangen_US
dc.contributor.authorLai, Lee-Jeneen_US
dc.date.accessioned2015-12-02T02:59:20Z-
dc.date.available2015-12-02T02:59:20Z-
dc.date.issued2015-07-01en_US
dc.identifier.issn0887-8013en_US
dc.identifier.urihttp://dx.doi.org/10.1002/jcla.21766en_US
dc.identifier.urihttp://hdl.handle.net/11536/128061-
dc.description.abstractBackgroundSynchrotron radiation infrared (SR-IR) microspectroscopy and SR-IR spectroscopic imaging are extremely valuable techniques for determining the molecular composition of biological and biomedical samples. In this work, SR-IR is applied in the study of the lung cancer cells in different cell cycles. MethodsWe use a novel synchrotron based radiation infrared system combined synchronized model human lung carcinoma to reveal its unique character pattern. ResultsAfter using SR-IR microspectroscopy, we discovered that the ratio of protein to lipid in G1 and G2 states is around 4.0 and 6.1, respectively. Moreover, for the DNA at the wavenumber position of 1225 cm(-1), the intensity ratio of G2 state to G1 state is approximately 1.6. These data indicate that the cell in G1 state has more lipid composition to prepare for the DNA synthesis, but the cell in G2 state has more protein composition to prepare for the mitosis. The cell has larger DNA concentration in G2 state, which can be explained for the DNA synthesis. ConclusionThrough our research, we demonstrate that different growth state of cancer cell presenting unique functional groups concentration profiles and distribution via using SR-IR microspectrometry. These applications will provide another ways to improve modern cancer screening in the future.en_US
dc.language.isoen_USen_US
dc.subjectcell cycleen_US
dc.subjectlung carcinomaen_US
dc.subjectmicrospectrometryen_US
dc.subjectsynchrotronen_US
dc.subjectsynchrotron radiation infrareden_US
dc.titleUsing Novel Method to Detect Different Cancer-Cell Stages of Model Human Lung Carcinomaen_US
dc.typeArticleen_US
dc.identifier.doi10.1002/jcla.21766en_US
dc.identifier.journalJOURNAL OF CLINICAL LABORATORY ANALYSISen_US
dc.citation.volume29en_US
dc.citation.spage285en_US
dc.citation.epage288en_US
dc.contributor.department材料科學與工程學系zh_TW
dc.contributor.departmentDepartment of Materials Science and Engineeringen_US
dc.identifier.wosnumberWOS:000358250300007en_US
dc.citation.woscount0en_US
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