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A prediction model for distinguishing lung squamous cell carcinoma from adenocarcinoma.
Li, Hui; Jiang, Zhengran; Leng, Qixin; Bai, Fan; Wang, Juan; Ding, Xiaosong; Li, Yuehong; Zhang, Xianghong; Fang, HongBin; Yfantis, Harris G; Xing, Lingxiao; Jiang, Feng.
Afiliação
  • Li H; Department of Pathology, Hebei Medical University, Shijiazhuang, Hebei, China.
  • Jiang Z; Department of Pathology, the University of Maryland School of Medicine, Baltimore, Maryland, USA.
  • Leng Q; The F. Edward Hébert School of Medicine at the Uniformed Services University of the Health Sciences, Bethesda, Maryland, USA.
  • Bai F; Department of Pathology, the University of Maryland School of Medicine, Baltimore, Maryland, USA.
  • Wang J; Department of Pathology, Hebei Medical University, Shijiazhuang, Hebei, China.
  • Ding X; Department of Pathology, Second Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.
  • Li Y; Department of Pathology, Hebei Medical University, Shijiazhuang, Hebei, China.
  • Zhang X; Department of Pathology, Second Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.
  • Fang H; Department of Pathology, Hebei Medical University, Shijiazhuang, Hebei, China.
  • Yfantis HG; Department of Pathology, Second Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.
  • Xing L; Department of Biostatistics, Bioinformatics and Biomathematics, Georgetown University Medical Center, Washington, D.C., USA.
  • Jiang F; Pathology and Laboratory Medicine, Baltimore Veterans Affairs Medical Center, Baltimore, Maryland, USA.
Oncotarget ; 8(31): 50704-50714, 2017 Aug 01.
Article em En | MEDLINE | ID: mdl-28881596
ABSTRACT
Accurate classification of squamous cell carcinoma (SCC) from adenocarcinoma (AC) of non-small cell lung cancer (NSCLC) can lead to personalized treatments of lung cancer. We aimed to develop a miRNA-based prediction model for differentiating SCC from AC in surgical resected tissues and bronchoalveolar lavage (BAL) samples. Expression levels of seven histological subtype-associated miRNAs were determined in 128 snap-frozen surgical lung tumor specimens by using reverse transcription-polymerase chain reaction (RT-PCR) to develop an optimal panel of miRNAs for acutely distinguishing SCC from AC. The biomarkers were validated in an independent cohort of 112 FFPE lung tumor tissues, and a cohort of 127 BAL specimens by using droplet digital PCR for differentiating SCC from AC. A prediction model with two miRNAs (miRs-205-5p and 944) was developed that had 0.988 area under the curve (AUC) with 96.55% sensitivity and 96.43% specificity for differentiating SCC from AC in frozen tissues, and 0.997 AUC with 96.43% sensitivity and 96.43% specificity in FFPE specimens. The diagnostic performance of the prediction model was reproducibly validated in BAL specimens for distinguishing SCC from AC with a higher accuracy compared with cytology (95.69 vs. 68.10%; P < 0.05). The prediction model might have a clinical value for accurately discriminating SCC from AC in both surgical lung tumor tissues and liquid cytological specimens.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Oncotarget Ano de publicação: 2017 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Oncotarget Ano de publicação: 2017 Tipo de documento: Article País de afiliação: China