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Detection of ALK rearrangements in lung cancer patients using a homebrew PCR assay.
Yu, Hui; Chang, JianHua; Liu, Fang; Wang, Qifeng; Lu, YongMing; Zhang, ZhuanXu; Shen, Jiabing; Zhai, Qing; Meng, Xia; Wang, Jialei; Ye, Xun.
Afiliación
  • Yu H; Department of Medical Oncology, Fudan University Shanghai Cancer Center, Shanghai, China.
  • Chang J; Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, China.
  • Liu F; Department of Medical Oncology, Fudan University Shanghai Cancer Center, Shanghai, China.
  • Wang Q; Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, China.
  • Lu Y; Department of Pharmacy, Fudan University Shanghai Cancer Center, Shanghai, China.
  • Zhang Z; Department of Pathology, Fudan University Shanghai Cancer Center, Shanghai, China.
  • Shen J; Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, China.
  • Zhai Q; Department of Pathology, Fudan University Shanghai Cancer Center, Shanghai, China.
  • Meng X; Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, China.
  • Wang J; Tissue bank, Fudan University Shanghai Cancer Center, Shanghai, China.
  • Ye X; Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, China.
Oncotarget ; 8(5): 7722-7728, 2017 Jan 31.
Article en En | MEDLINE | ID: mdl-28032602
Lung cancer patients with anaplastic lymphoma kinase (ALK) rearrangements are candidates for targeted therapeutics. However, patients must be tested with a companion diagnostic assay to realize their ALK rearrangement status. We analyzed the publicly available E-GEOD-31210 microarray dataset and identified a non-coding RNA, sweyjawbu, which is strongly associated with ALK rearrangements. We validated these results using quantitative real-time PCR in an independent cohort consisting of 4 cell lines and 83 clinical samples. We could differentiate between ALK rearrangement-positive and -negative lung cancer samples by comparing sweyjawbu expression. Additionally, ALK rearrangement status was determined by comparing the expression of the 5' and 3' regions of the ALK transcript or by detecting known ALK hybrid subtypes. Thus, using our homebrew PCR assay, we were able to accurately detect ALK rearrangements, which could be used for diagnostic screening of lung cancer patients. The prototype could potentially be transferred to an automatic multiplex PCR platform (FilmArray) to differentiate between ALK rearrangement-positive and -negative patients in point-of-care settings.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Reordenamiento Génico / Biomarcadores de Tumor / Proteínas Tirosina Quinasas Receptoras / Reacción en Cadena de la Polimerasa de Transcriptasa Inversa / Detección Precoz del Cáncer / Reacción en Cadena en Tiempo Real de la Polimerasa / Neoplasias Pulmonares Tipo de estudio: Diagnostic_studies / Screening_studies Límite: Humans Idioma: En Revista: Oncotarget Año: 2017 Tipo del documento: Article País de afiliación: China Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Reordenamiento Génico / Biomarcadores de Tumor / Proteínas Tirosina Quinasas Receptoras / Reacción en Cadena de la Polimerasa de Transcriptasa Inversa / Detección Precoz del Cáncer / Reacción en Cadena en Tiempo Real de la Polimerasa / Neoplasias Pulmonares Tipo de estudio: Diagnostic_studies / Screening_studies Límite: Humans Idioma: En Revista: Oncotarget Año: 2017 Tipo del documento: Article País de afiliación: China Pais de publicación: Estados Unidos