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Longitudinal monitoring reveals dynamic changes in circulating tumor cells (CTCs) and CTC-associated miRNAs in response to chemotherapy in metastatic colorectal cancer patients.
Tan, Karen; Leong, Sai Mun; Kee, Zizheng; Caramat, Patrick Vincent; Teo, James; Blanco, Michael Vito Martin; Koay, Evelyn S C; Cheong, Wai Kit; Soh, Thomas I-Peng; Yong, Wei Peng; Pang, Angela.
Afiliação
  • Tan K; Department of Laboratory Medicine, National University Hospital, Singapore. Electronic address: karen_ml_tan@nuhs.edu.sg.
  • Leong SM; Department of Pathology, National University, Singapore.
  • Kee Z; Department of Pathology, National University, Singapore.
  • Caramat PV; Department of Laboratory Medicine, National University Hospital, Singapore.
  • Teo J; Department of Laboratory Medicine, National University Hospital, Singapore.
  • Blanco MVM; National University Cancer Institute, Singapore.
  • Koay ESC; Department of Pathology, National University, Singapore.
  • Cheong WK; Department of Surgery, National University Hospital, Singapore.
  • Soh TI; National University Cancer Institute, Singapore.
  • Yong WP; National University Cancer Institute, Singapore.
  • Pang A; National University Cancer Institute, Singapore. Electronic address: angela_pang@nuhs.com.sg.
Cancer Lett ; 423: 1-8, 2018 06 01.
Article em En | MEDLINE | ID: mdl-29518480
We evaluated the changes in CTC count and CTC-associated miRNAs during the course of chemotherapy in patients with metastatic colorectal cancer. Blood samples were collected from 9 metastatic colorectal cancer patients prior to chemotherapy and at every other chemotherapy session during the course of treatment. CTCs were isolated and enumerated using a size-exclusion method (CellSievo, Singapore). CTC-associated miRNAs were isolated using a paper-based, partitioning method, and analyzed using reverse transcription quantitative real-time PCR (MiRXES, Singapore). CTC count trends generally correlated with disease progression defined by radiological measurements and trends in carcinoembryonic antigen (CEA) levels; hence CTC counts may be useful in cases where CEA is not elevated. CTC-associated miRNAs identified were miR-15b, miR-16, miR-19a, miR-21, miR-25, miR-30d, miR-126, miR-185, miR-221, miR-222, and miR-324-5p. The expression of CTC-associated miRNAs did not appear to correlate with CTC count and exhibited inter-individual heterogeneity. This pilot study suggests that analysis of CTC changes during the course of treatment may be useful in monitoring response to therapy in metastatic colorectal cancer.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Protocolos de Quimioterapia Combinada Antineoplásica / MicroRNAs / Células Neoplásicas Circulantes Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Cancer Lett Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Protocolos de Quimioterapia Combinada Antineoplásica / MicroRNAs / Células Neoplásicas Circulantes Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Cancer Lett Ano de publicação: 2018 Tipo de documento: Article