Comparison of Circulating miRNAs Expression Alterations in Matched Tissue and Plasma Samples During Colorectal Cancer Progression.


Journal

Pathology oncology research : POR
ISSN: 1532-2807
Titre abrégé: Pathol Oncol Res
Pays: Switzerland
ID NLM: 9706087

Informations de publication

Date de publication:
Jan 2019
Historique:
received: 24 08 2017
accepted: 12 09 2017
pubmed: 6 10 2017
medline: 13 2 2019
entrez: 6 10 2017
Statut: ppublish

Résumé

MicroRNAs (miRNAs) have been found to play a critical role in colorectal adenoma-carcinoma sequence. MiRNA-specific high-throughput arrays became available to detect promising miRNA expression alterations even in biological fluids, such as plasma samples, where miRNAs are stable. The purpose of this study was to identify circulating miRNAs showing altered expression between normal colonic (N), tubular adenoma (ADT), tubulovillous adenoma (ADTV) and colorectal cancer (CRC) matched plasma and tissue samples. Sixteen peripheral plasma and matched tissue biopsy samples (N n = 4; ADT n = 4; ADTV n = 4; CRC n = 4) were selected, and total RNA including miRNA fraction was isolated. MiRNAs from plasma samples were extracted using QIAamp Circulating Nucleic Acid Kit (Qiagen). Matched tissue-plasma miRNA microarray experiments were conducted by GeneChip® miRNA 3.0 Array (Affymetrix). RT-qPCR (microRNA Ready-to-use PCR Human Panel I + II; Exiqon) was used for validation. Characteristic miRNA expression alterations were observed in comparison of AD and CRC groups (miR-149*, miR-3196, miR-4687) in plasma samples. In the N vs. CRC comparison, significant overexpression of miR-612, miR-1296, miR-933, miR-937 and miR-1207 was detected by RT-PCR (p < 0.05). Similar expression pattern of these miRNAs were observed using microarray in tissue pairs, as well. Although miRNAs were also found in circulatory system in a lower concentration compared to tissues, expression patterns slightly overlapped between tissue and plasma samples. Detected circulating miRNA alterations may originate not only from the primer tumor but from other cell types including immune cells.

Identifiants

pubmed: 28980150
doi: 10.1007/s12253-017-0308-1
pii: 10.1007/s12253-017-0308-1
doi:

Substances chimiques

Biomarkers, Tumor 0
Circulating MicroRNA 0

Types de publication

Comparative Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

97-105

Subventions

Organisme : National Research, Development and Innovation Office
ID : KMR-12-1-2012-0216
Organisme : Országos Tudományos Kutatási Alapprogramok
ID : OTKA-K111743

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Auteurs

Zsófia Brigitta Nagy (ZB)

Molecular Gastroenterology Laboratory, 2nd Department of Internal Medicine, Semmelweis University, Szentkirályi street 46, Budapest, 1088, Hungary. nagyzsofiab@gmail.com.

Barbara Kinga Barták (BK)

Molecular Gastroenterology Laboratory, 2nd Department of Internal Medicine, Semmelweis University, Szentkirályi street 46, Budapest, 1088, Hungary.

Alexandra Kalmár (A)

Molecular Gastroenterology Laboratory, 2nd Department of Internal Medicine, Semmelweis University, Szentkirályi street 46, Budapest, 1088, Hungary.

Orsolya Galamb (O)

Molecular Gastroenterology Laboratory, 2nd Department of Internal Medicine, Semmelweis University, Szentkirályi street 46, Budapest, 1088, Hungary.
Molecular Medicine Research Group, Hungarian Academy of Sciences, Budapest, Hungary.

Barnabás Wichmann (B)

Molecular Gastroenterology Laboratory, 2nd Department of Internal Medicine, Semmelweis University, Szentkirályi street 46, Budapest, 1088, Hungary.
Molecular Medicine Research Group, Hungarian Academy of Sciences, Budapest, Hungary.

Magdolna Dank (M)

Department of Clinical Oncology, Semmelweis University, Budapest, Hungary.

Péter Igaz (P)

Molecular Gastroenterology Laboratory, 2nd Department of Internal Medicine, Semmelweis University, Szentkirályi street 46, Budapest, 1088, Hungary.
Molecular Medicine Research Group, Hungarian Academy of Sciences, Budapest, Hungary.

Zsolt Tulassay (Z)

Molecular Gastroenterology Laboratory, 2nd Department of Internal Medicine, Semmelweis University, Szentkirályi street 46, Budapest, 1088, Hungary.
Molecular Medicine Research Group, Hungarian Academy of Sciences, Budapest, Hungary.

Béla Molnár (B)

Molecular Gastroenterology Laboratory, 2nd Department of Internal Medicine, Semmelweis University, Szentkirályi street 46, Budapest, 1088, Hungary.
Molecular Medicine Research Group, Hungarian Academy of Sciences, Budapest, Hungary.

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