Delivery of platelet TPM3 mRNA into breast cancer cells via microvesicles enhances metastasis

Platelets are implicated in the pathophysiology of breast and other cancers through their role in exchanging biomolecules with tumor cells in the tumor microenvironment. Such exchange results in tumor‐educated platelets with altered RNA expression profiles. Multiple lines of evidence indicate that p...

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Main Authors: Bing Yao, Shuang Qu, Ruifeng Hu, Wen Gao, Shidai Jin, Junyi Ju, Quan Zhao
Format: Article
Language:English
Published: Wiley 2019-12-01
Series:FEBS Open Bio
Subjects:
Online Access:https://doi.org/10.1002/2211-5463.12759
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author Bing Yao
Shuang Qu
Ruifeng Hu
Wen Gao
Shidai Jin
Junyi Ju
Quan Zhao
author_facet Bing Yao
Shuang Qu
Ruifeng Hu
Wen Gao
Shidai Jin
Junyi Ju
Quan Zhao
author_sort Bing Yao
collection DOAJ
description Platelets are implicated in the pathophysiology of breast and other cancers through their role in exchanging biomolecules with tumor cells in the tumor microenvironment. Such exchange results in tumor‐educated platelets with altered RNA expression profiles. Multiple lines of evidence indicate that platelet RNA profiles may be suitable as diagnostic biomarkers for cancer‐related biological processes. In this study, we characterized the gene expression signatures of platelets in breast cancer (BC) by high‐throughput sequencing and quantitative real‐time RT‐PCR. Our results indicate that the expression of TPM3 (tropomyosin 3) mRNA is significantly elevated in platelets from patients with BC compared with age‐matched healthy control subjects. Furthermore, up‐regulation of TPM3 mRNA in platelets was found to be significantly correlated with metastasis in patients with BC. Finally, we report that platelet TPM3 mRNA is delivered into BC cells through microvesicles and leads to enhanced migrative phenotype of BC cells. In summary, our findings suggest that the transfer of platelet TPM3 mRNA into cancer cells via microvesicles promotes cancer cell migration, and thus platelet‐derived TPM3 mRNA may be a suitable biomarker for early diagnosis of metastatic BC.
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spelling doaj.art-3af745915af542e780e9287aa73d08002023-11-21T07:01:44ZengWileyFEBS Open Bio2211-54632019-12-019122159216910.1002/2211-5463.12759Delivery of platelet TPM3 mRNA into breast cancer cells via microvesicles enhances metastasisBing Yao0Shuang Qu1Ruifeng Hu2Wen Gao3Shidai Jin4Junyi Ju5Quan Zhao6The State Key Laboratory of Pharmaceutical Biotechnology School of Life Sciences Nanjing University ChinaThe State Key Laboratory of Pharmaceutical Biotechnology School of Life Sciences Nanjing University ChinaThe State Key Laboratory of Pharmaceutical Biotechnology School of Life Sciences Nanjing University ChinaDepartment of Oncology The First Affiliated Hospital of Nanjing Medical University ChinaDepartment of Oncology The First Affiliated Hospital of Nanjing Medical University ChinaThe State Key Laboratory of Pharmaceutical Biotechnology School of Life Sciences Nanjing University ChinaThe State Key Laboratory of Pharmaceutical Biotechnology School of Life Sciences Nanjing University ChinaPlatelets are implicated in the pathophysiology of breast and other cancers through their role in exchanging biomolecules with tumor cells in the tumor microenvironment. Such exchange results in tumor‐educated platelets with altered RNA expression profiles. Multiple lines of evidence indicate that platelet RNA profiles may be suitable as diagnostic biomarkers for cancer‐related biological processes. In this study, we characterized the gene expression signatures of platelets in breast cancer (BC) by high‐throughput sequencing and quantitative real‐time RT‐PCR. Our results indicate that the expression of TPM3 (tropomyosin 3) mRNA is significantly elevated in platelets from patients with BC compared with age‐matched healthy control subjects. Furthermore, up‐regulation of TPM3 mRNA in platelets was found to be significantly correlated with metastasis in patients with BC. Finally, we report that platelet TPM3 mRNA is delivered into BC cells through microvesicles and leads to enhanced migrative phenotype of BC cells. In summary, our findings suggest that the transfer of platelet TPM3 mRNA into cancer cells via microvesicles promotes cancer cell migration, and thus platelet‐derived TPM3 mRNA may be a suitable biomarker for early diagnosis of metastatic BC.https://doi.org/10.1002/2211-5463.12759biomarkerbreast cancerplateletRNATPM3
spellingShingle Bing Yao
Shuang Qu
Ruifeng Hu
Wen Gao
Shidai Jin
Junyi Ju
Quan Zhao
Delivery of platelet TPM3 mRNA into breast cancer cells via microvesicles enhances metastasis
FEBS Open Bio
biomarker
breast cancer
platelet
RNA
TPM3
title Delivery of platelet TPM3 mRNA into breast cancer cells via microvesicles enhances metastasis
title_full Delivery of platelet TPM3 mRNA into breast cancer cells via microvesicles enhances metastasis
title_fullStr Delivery of platelet TPM3 mRNA into breast cancer cells via microvesicles enhances metastasis
title_full_unstemmed Delivery of platelet TPM3 mRNA into breast cancer cells via microvesicles enhances metastasis
title_short Delivery of platelet TPM3 mRNA into breast cancer cells via microvesicles enhances metastasis
title_sort delivery of platelet tpm3 mrna into breast cancer cells via microvesicles enhances metastasis
topic biomarker
breast cancer
platelet
RNA
TPM3
url https://doi.org/10.1002/2211-5463.12759
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