Author:
Shimada Yoshihisa,Yoshioka Yusuke,Kudo Yujin,Mimae Takahiro,Miyata Yoshihiro,Adachi Hiroyuki,Ito Hiroyuki,Okada Morihito,Ohira Tatsuo,Matsubayashi Jun,Ochiya Takahiro,Ikeda Norihiko
Abstract
AbstractLymphovascular invasion (LVI) is a fundamental step toward the spread of cancer. Extracellular vesicles (EVs) promote cellular communication by shuttling cargo, such as microRNAs (miRNAs). However, whether EV-associated miRNAs serve as biomarkers for LVI remains unclear. This study aimed to identify EV-associated miRNAs related to LVI and validate the miRNA levels from patients with early-stage lung adenocarcinoma (LADC). Blood samples were collected from patients undergoing pulmonary resection for stage I LADC before surgery. The patients were classified into three groups according to the presence of LVI and postoperative recurrence. Serum-derived EVs in the derivation cohort were used for small RNA sequencing, while the selected LVI miRNA candidates were validated via real-time quantitative polymerase chain reaction using 44 patient and 16 healthy donor samples as the validation cohorts. Five miRNAs (miR-99b-3p, miR-26a-5p, miR-93-5p, miR-30d-5p, and miR-365b-3p) were assessed, and miR-30d-5p (p = 0.036) levels were significantly downregulated in the LVI-positive group. miR-30d-5p levels in healthy donors were lower than those in LADC patients. Patients with high miR-30d-5p levels had favorable survival compared to those with low miR-30d-5p levels. miR-30d-5p level in EVs may serve as a promising biomarker for detecting LVI in patients with early-stage LADC.
Funder
a Grant-in-Aid for Cancer Research from the Ministry of Education, Culture, Sports and Technology
Project for Cancer Research and Therapeutic Evolution
the Project for Cancer Research and Therapeutic Evolution
Publisher
Springer Science and Business Media LLC
Cited by
4 articles.
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