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dc.contributor.authorSpringer, Simeon U.
dc.contributor.authorChen, Chung-Hsin
dc.contributor.authorPena, Maria Del Carmen Rodriguez
dc.contributor.authorLi, Lu
dc.contributor.authorDouville, Christopher
dc.contributor.authorWang, Yuxuan
dc.contributor.authorCohen, Joshua David
dc.contributor.authorTaheri, Diana
dc.contributor.authorSilliman, Natalie
dc.contributor.authorSchaefer, Joy
dc.contributor.authorPtak, Janine
dc.contributor.authorDobbyn, Lisa
dc.contributor.authorPapoli, Maria
dc.contributor.authorKinde, Isaac
dc.contributor.authorAfsari, Bahman
dc.contributor.authorTregnago, Aline C.
dc.contributor.authorBezerra, Stephania M.
dc.contributor.authorVandenBussche, Christopher
dc.contributor.authorFujita, Kazutoshi
dc.contributor.authorErtoy, Dilek
dc.contributor.authorCunha, Isabela W.
dc.contributor.authorYu, Lijia
dc.contributor.authorBivalacqua, Trinity J.
dc.contributor.authorGrollman, Arthur P.
dc.contributor.authorDiaz, Luis A.
dc.contributor.authorKarchin, Rachel
dc.contributor.authorDanilova, Ludmila
dc.contributor.authorHuang, Chao-Yuan
dc.contributor.authorShun, Chia-Tung
dc.contributor.authorTuresky, Robert J.
dc.contributor.authorYun, Byeong Hwa
dc.contributor.authorRosenquist, Thomas A.
dc.contributor.authorPu, Yeong-Shiau
dc.contributor.authorHruban, Ralph H.
dc.contributor.authorTomasetti, Cristian
dc.contributor.authorPapadopoulos, Nickolas
dc.contributor.authorKinzler, Ken W.
dc.contributor.authorVogelstein, Bert
dc.contributor.authorDickman, Kathleen G.
dc.contributor.authorNetto, George J.
dc.date.accessioned2019-12-12T06:43:30Z
dc.date.available2019-12-12T06:43:30Z
dc.date.issued2018
dc.identifier.issn2050-084X
dc.identifier.urihttps://doi.org/10.7554/eLife.32143
dc.identifier.urihttp://hdl.handle.net/11655/16812
dc.description.abstractCurrent non-invasive approaches for detection of urothelial cancers are suboptimal. We developed a test to detect urothelial neoplasms using DNA recovered from cells shed into urine. UroSEEK incorporates massive parallel sequencing assays for mutations in 11 genes and copy number changes on 39 chromosome arms. In 570 patients at risk for bladder cancer ( BC), UroSEEK was positive in 83% of those who developed BC. Combined with cytology, UroSEEK detected 95% of patients who developed BC. Of 56 patients with upper tract urothelial cancer, 75% tested positive by UroSEEK, including 79% of those with non-invasive tumors. UroSEEK detected genetic abnormalities in 68% of urines obtained from BC patients under surveillance who demonstrated clinical evidence of recurrence. The advantages of UroSEEK over cytology were evident in low-grade BCs; UroSEEK detected 67% of cases whereas cytology detected none. These results establish the foundation for a new non-invasive approach for detection of urothelial cancer.
dc.language.isoen
dc.publisherElife Sciences Publications Ltd
dc.relation.isversionof10.7554/eLife.32143
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectLife Sciences & Biomedicine - Other Topics
dc.titleNon-Invasive Detection Of Urothelial Cancer Through The Analysis Of Driver Gene Mutations And Aneuploidy
dc.typeinfo:eu-repo/semantics/article
dc.relation.journalElife
dc.contributor.departmentTıbbi Patoloji
dc.identifier.volume7
dc.description.indexWoS
dc.description.indexScopus


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