Methionine Restriction Increases Exosome Production and Secretion in Breast Cancer Cells.

IF 2.6 4区 医学 Q2 GENETICS & HEREDITY
Sachiko Inubushi, Tomonari Kunihisa, Sachiko Mizumoto, Shotaro Inoue, Mayuko Miki, Atsushi Suetsugu, Hirokazu Tanino, Robert M Hoffman
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引用次数: 0

Abstract

Background/aim: Methionine addiction is the elevated requirement for exogenous methionine for growth and survival of cancer cells, termed the Hoffman effect. Methionine-addicted cancer cells synthesize normal or excess amounts of methionine but still need an external source of methionine. Methionine restriction (MR) by either a methionine-free medium or in vivo by a low-methionine diet or by methioninase, selectively arrests cancer cells in the late S/G2 cell cycle phase, but not normal cells. The present study focuses on the comparison of production and secretion of exosomes by cancer cells under MR and normal conditions.

Materials and methods: MDA-MB-231 cells (triple-negative breast cancer), containing exosomes labeled with CD63-GFP (CD63-GFP exosomes), were visualized by fluorescence microscopy. MDA-MB-231 cells expressing exosome-specific CD63-GFP were cultured in methionine-containing (MET+) or in methionine-free (MET-) DMEM conditions. Exosomes were isolated from conditioned medium of cultured MDA-MD-231 cells by ultracentrifugation and characterized by nanoparticle tracking analysis (NTA) and Western blotting.

Results: When MDA-MB-231-CD63-GFP cells were cultured under MR conditions, they arrested their growth and CD63-GFP-expressing exosomes were strongly increased in the cells. MR resulted in approximately a 2-fold increase in exosome production and secretion per cell, even though cell growth was arrested. Methionine restriction thus resulted in elevated exosome production and secretion per surviving cell.

Conclusion: Exosome production and secretion in the cancer cells increased under MR, suggesting a relation between MR and exosome production and secretion.

甲硫氨酸限制增加乳腺癌症细胞外泌体的产生和分泌。
背景/目的:甲硫氨酸成瘾是癌症细胞生长和存活对外源性甲硫氨酸的需求增加,称为霍夫曼效应。甲硫氨酸成瘾的癌症细胞合成正常或过量的甲硫氨酸,但仍需要甲硫氨酸的外部来源。通过无甲硫氨酸培养基或通过低甲硫氨酸饮食或通过甲硫氨酸酶的体内甲硫氨酸限制(MR),选择性地阻止处于S/G2细胞周期后期的癌症细胞,但不阻止正常细胞。本研究的重点是比较癌症细胞在MR和正常条件下外泌体的产生和分泌。材料和方法:通过荧光显微镜观察含有CD63-GFP标记的外泌体(CD63-GFP-外泌体)的MDA-MB-231细胞(癌症三阴性乳腺癌)。表达外泌体特异性CD63-GFP的MDA-MB-231细胞在含蛋氨酸(MET+)或不含蛋氨酸(MET-)的DMEM条件下培养。通过超速离心从培养的MDA-MD-231细胞的条件培养基中分离外泌体,并通过纳米粒子跟踪分析(NTA)和蛋白质印迹进行表征。结果:当MDA-MB-231-CD63-GFP细胞在MR条件下培养时,它们停止了生长,并且表达CD63GFP的外泌体在细胞中强烈增加。MR导致每个细胞的外泌体产生和分泌增加约2倍,即使细胞生长被抑制。因此,蛋氨酸限制导致每个存活细胞的外泌体产生和分泌增加。结论:在磁共振作用下,癌症细胞外泌体的产生和分泌增加,提示磁共振与外泌体产生和分泌之间存在一定的关系。
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来源期刊
Cancer Genomics & Proteomics
Cancer Genomics & Proteomics ONCOLOGY-GENETICS & HEREDITY
CiteScore
5.00
自引率
8.00%
发文量
51
期刊介绍: Cancer Genomics & Proteomics (CGP) is an international peer-reviewed journal designed to publish rapidly high quality articles and reviews on the application of genomic and proteomic technology to basic, experimental and clinical cancer research. In this site you may find information concerning the editorial board, editorial policy, issue contents, subscriptions, submission of manuscripts and advertising. The first issue of CGP circulated in January 2004. Cancer Genomics & Proteomics is a journal of the International Institute of Anticancer Research. From January 2013 CGP is converted to an online-only open access journal. Cancer Genomics & Proteomics supports (a) the aims and the research projects of the INTERNATIONAL INSTITUTE OF ANTICANCER RESEARCH and (b) the organization of the INTERNATIONAL CONFERENCES OF ANTICANCER RESEARCH.
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