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Advances in Keratin 17 as a Cancer Biomarker: A Systematic Review
Advances in Keratin 17 as a Cancer Biomarker: A Systematic Review
Advances in Keratin 17 as a Cancer Biomarker: A Systematic Review

상세정보

자료유형  
 학위논문 서양
최종처리일시  
20250211151054
ISBN  
9798382321417
DDC  
610
저자명  
Tseng, Robert.
서명/저자  
Advances in Keratin 17 as a Cancer Biomarker: A Systematic Review
발행사항  
[Sl] : Yale University, 2024
발행사항  
Ann Arbor : ProQuest Dissertations & Theses, 2024
형태사항  
87 p
주기사항  
Source: Dissertations Abstracts International, Volume: 85-11, Section: B.
주기사항  
Advisor: Escobar-Hoyos, Luisa F.;Shroyer, Kenneth R.
학위논문주기  
Thesis (M.D.)--Yale University, 2024.
초록/해제  
요약Background: In an era where tumor heterogeneity leads to widely variable cancer treatment outcomes, there is an unmet need for biomarkers that can characterize tumor subtypes, inform prognosis, and guide clinical decision-making for therapy. As an oncofetal monofilament that is only expressed in embryonic and cancer tissue, keratin 17 (K17) has been demonstrated as an effective biomarker in a wide variety of cancer types, detection methods, and clinical purposes. In order to guide and inform future investigations on K17, we performed a systematic review of clinical studies assessing the effectiveness of K17 as a cancer biomarker.Methods: We performed a literature search of relevant articles reporting K17 as a cancer biomarker prior to December 16th, 2023. After manual review, we assigned articles to diagnostic, prognostic, and predictive study categories. We extracted relevant diagnostic and prognostic statistics, experimental methodologies, and co-examined biomarkers. Additionally, we performed bias analysis utilizing data reported from prognostic studies. Finally, using RNA-seq samples of tumor and normal tissue specimens from The Cancer Genome Atlas (TCGA) and Genotype-Tissue Expression (GTEx) portal, we perform our own diagnostic analysis across 21 tumor/normal tissue pairs, as well as Kaplan-Meier analysis across 32 cancer types.Results: Of the 453 studies identified in our literature search, we obtained 40 diagnostic, 50 prognostic, and 5 predictive studies. Altogether, we summarized the methodologies of 37 diagnostic studies and ROC (Receiver Operating Curve) analyses provided by 15 articles. Our review suggests that K17 is a highly applicable diagnostic biomarker, characterizable by multiple assay types, to distinguish either malignant from normal pathology, or two different malignant pathologies. For prognostic studies, we extracted Cox proportional hazards models provided by 36 studies, a majority of which suggest that K17 is a negatively prognostic biomarker in a wide range of cancer types, including oropharyngeal, esophageal, gastric, pancreatic, gallbladder, ovarian, and endometrial cancers. Finally, based on our review, K17 is predictive of inferior response to therapy in 4 out of 5 predictive studies.Conclusion: K17 is a widely applicable cancer biomarker that has been shown to be effective in diagnostic settings, and increasingly in patient specimens obtained non-invasively. As both an IHC and RNA-based biomarker, K17 is widely associated with negative prognosis. New predictive studies are beginning to correlate K17 to inferior chemotherapeutic and immunotherapeutic treatment response.
일반주제명  
Medicine
일반주제명  
Molecular biology
일반주제명  
Oncology
키워드  
Cancer treatment
키워드  
Tumor heterogeneity
키워드  
Keratin 17
키워드  
Biomarkers
기타저자  
Yale University Yale School of Medicine
기본자료저록  
Dissertations Abstracts International. 85-11B.
전자적 위치 및 접속  
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■035    ▼a(MiAaPQ)AAI31141983
■040    ▼aMiAaPQ▼cMiAaPQ
■0820  ▼a610
■1001  ▼aTseng,  Robert.
■24510▼aAdvances  in  Keratin  17  as  a  Cancer  Biomarker:  A  Systematic  Review
■260    ▼a[Sl]▼bYale  University▼c2024
■260  1▼aAnn  Arbor▼bProQuest  Dissertations  &  Theses▼c2024
■300    ▼a87  p
■500    ▼aSource:  Dissertations  Abstracts  International,  Volume:  85-11,  Section:  B.
■500    ▼aAdvisor:  Escobar-Hoyos,  Luisa  F.;Shroyer,  Kenneth  R.
■5021  ▼aThesis  (M.D.)--Yale  University,  2024.
■520    ▼aBackground:  In  an  era  where  tumor  heterogeneity  leads  to  widely  variable  cancer  treatment  outcomes,  there  is  an  unmet  need  for  biomarkers  that  can  characterize  tumor  subtypes,  inform  prognosis,  and  guide  clinical  decision-making  for  therapy.  As  an  oncofetal  monofilament  that  is  only  expressed  in  embryonic  and  cancer  tissue,  keratin  17  (K17)  has  been  demonstrated  as  an  effective  biomarker  in  a  wide  variety  of  cancer  types,  detection  methods,  and  clinical  purposes.  In  order  to  guide  and  inform  future  investigations  on  K17,  we  performed  a  systematic  review  of  clinical  studies  assessing  the  effectiveness  of  K17  as  a  cancer  biomarker.Methods:  We  performed  a  literature  search  of  relevant  articles  reporting  K17  as  a  cancer  biomarker  prior  to  December  16th,  2023.  After  manual  review,  we  assigned  articles  to  diagnostic,  prognostic,  and  predictive  study  categories.  We  extracted  relevant  diagnostic  and  prognostic  statistics,  experimental  methodologies,  and  co-examined  biomarkers.  Additionally,  we  performed  bias  analysis  utilizing  data  reported  from  prognostic  studies.  Finally,  using  RNA-seq  samples  of  tumor  and  normal  tissue  specimens  from  The  Cancer  Genome  Atlas  (TCGA)  and  Genotype-Tissue  Expression  (GTEx)  portal,  we  perform  our  own  diagnostic  analysis  across  21  tumor/normal  tissue  pairs,  as  well  as  Kaplan-Meier  analysis  across  32  cancer  types.Results:  Of  the  453  studies  identified  in  our  literature  search,  we  obtained  40  diagnostic,  50  prognostic,  and  5  predictive  studies.  Altogether,  we  summarized  the  methodologies  of  37  diagnostic  studies  and  ROC  (Receiver  Operating  Curve)  analyses  provided  by  15  articles.  Our  review  suggests  that  K17  is  a  highly  applicable  diagnostic  biomarker,  characterizable  by  multiple  assay  types,  to  distinguish  either  malignant  from  normal  pathology,  or  two  different  malignant  pathologies.  For  prognostic  studies,  we  extracted  Cox  proportional  hazards  models  provided  by  36  studies,  a  majority  of  which  suggest  that  K17  is  a  negatively  prognostic  biomarker  in  a  wide  range  of  cancer  types,  including  oropharyngeal,  esophageal,  gastric,  pancreatic,  gallbladder,  ovarian,  and  endometrial  cancers.  Finally,  based  on  our  review,  K17  is  predictive  of  inferior  response  to  therapy  in  4  out  of  5  predictive  studies.Conclusion:  K17  is  a  widely  applicable  cancer  biomarker  that  has  been  shown  to  be  effective  in  diagnostic  settings,  and  increasingly  in  patient  specimens  obtained  non-invasively.  As  both  an  IHC  and  RNA-based  biomarker,  K17  is  widely  associated  with  negative  prognosis.  New  predictive  studies  are  beginning  to  correlate  K17  to  inferior  chemotherapeutic  and  immunotherapeutic  treatment  response.
■590    ▼aSchool  code:  0265.
■650  4▼aMedicine
■650  4▼aMolecular  biology
■650  4▼aOncology
■653    ▼aCancer  treatment
■653    ▼aTumor  heterogeneity
■653    ▼aKeratin  17
■653    ▼aBiomarkers
■690    ▼a0564
■690    ▼a0307
■690    ▼a0992
■71020▼aYale  University▼bYale  School  of  Medicine.
■7730  ▼tDissertations  Abstracts  International▼g85-11B.
■790    ▼a0265
■791    ▼aM.D.
■792    ▼a2024
■793    ▼aEnglish
■85640▼uhttp://www.riss.kr/pdu/ddodLink.do?id=T17160645▼nKERIS▼z이  자료의  원문은  한국교육학술정보원에서  제공합니다.

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