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Erschienen in: Journal of Cancer Research and Clinical Oncology 11/2019

24.09.2019 | Original Article – Cancer Research

A three-platelet mRNA set: MAX, MTURN and HLA-B as biomarker for lung cancer

verfasst von: Lele Liu, Xingguo Song, Xinyi Li, Linlin Xue, Shanshan Ding, Limin Niu, Li Xie, Xianrang Song

Erschienen in: Journal of Cancer Research and Clinical Oncology | Ausgabe 11/2019

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Abstract

Background

During the development of tumors, tumors “educate” platelets causing changes in their mRNAs expression profiles and phenotypes, thereby, tumor-educated platelet (TEP) mRNA profile has the potential to diagnose lung cancer. The current study aimed to examine whether TEPs might be a potential biomarker for lung cancer diagnostics.

Methods

Platelet precipitation was obtained by low-speed centrifugation and subjected to Trizol for total RNA extraction. Platelet MAX, MTURN, and HLA-B mRNA were selected by microarray, validated by qPCR, and analyzed combined with related clinical factors.

Results

Our results showed that a three-platelet mRNA set: MAX, MTURN, and HLA-B was significantly up-regulated in lung cancer patients as well as in early-stage lung cancer patients compared with those from healthy donors, the area under the curve (AUC) was 0.734, 0.787, respectively, among which platelet MTURN mRNA processed a dramatically high diagnostic efficiency in female patients with lung cancer, its AUC for female was 0.825. More importantly, the three-platelet mRNA set: MAX, MTURN, and HLA-B was associated with chemotherapeutic effect, low mRNA expression of this three-platelet set was correlated with “favorable” first chemotherapy response.

Conclusions

A three-platelet mRNA set: MAX, MTURN and HLA-B enables blood-based lung cancer diagnosis and chemotherapy response prediction.
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Metadaten
Titel
A three-platelet mRNA set: MAX, MTURN and HLA-B as biomarker for lung cancer
verfasst von
Lele Liu
Xingguo Song
Xinyi Li
Linlin Xue
Shanshan Ding
Limin Niu
Li Xie
Xianrang Song
Publikationsdatum
24.09.2019
Verlag
Springer Berlin Heidelberg
Erschienen in
Journal of Cancer Research and Clinical Oncology / Ausgabe 11/2019
Print ISSN: 0171-5216
Elektronische ISSN: 1432-1335
DOI
https://doi.org/10.1007/s00432-019-03032-9

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