Changes in phospholipid metabolism in exosomes of hormone-sensitive and hormone-resistant prostate cancer cells.
Changes in phospholipid metabolism in exosomes of hormone-sensitive and hormone-resistant prostate cancer cells.
复制标题
激素敏感和激素抵抗性前列腺癌细胞外泌体磷脂代谢的变化
DOI:
10.7150/jca.48906
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发表时间:
2021
影响因子:
3.9
通讯作者:
Liu T
中科院分区:
文献类型:
--
作者:
Yi X;Li Y;Hu X;Wang F;Liu T
Background: To explore the changes in lipids in exosomes of hormone-sensitive and hormone-resistant prostate cancer cells and develop an inexpensive and rapid technique for screening lipid-based biomarkers of prostate cancer. Methods: Exosomes were extracted from LnCap, PC3 and DU-145 cells, and their lipid composition was analyzed quantitatively using high-throughput mass spectrometry. Exosomes released by LnCap prostate cancer cells were also purified using a modified procedure based on polyethylene glycol (PEG) precipitation. Results: Exosomes extracted from LnCap cells contained higher proportions of phosphatidyl choline, phosphatidyl ethanolamine and phosphatidyl inositol lipids than whole LnCap cells. Lysophosphatidylcholine, a harmful intermediate product of phosphatidylcholine metabolism in vivo, was not found in LnCap cells but in exosomes. Phospholipids were different in exosomes from LnCap, PC3 and DU-145 prostate cancer cells. The main lipid pathways involved, i.e., glycerophospholipid metabolism, autophagy, and ferroptosis pathways, were also different in these cells. Exosomes isolated by this modified PEG precipitation technique were similar in purity to those obtained using a commercial kit. Conclusions: This study demonstrates that phosphatidylcholine and its harmful product lysophosphatidylcholine may play important roles in hormone-sensitive prostate cancer. Phospholipid exosome metabolism was changed in hormone-sensitive and hormone-resistant prostate cancer cells. The LPC, lipid pathway of autophagy and ferroptosis may act as therapeutic targets. The possibility of purifying prostate cancer cell exosomes using modified PEG precipitation is suitable for cancer screening.
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影响因子:
168.9
作者:
Grönberg, H
通讯作者:
Grönberg, H
影响因子:
3.8
作者:
Li J;Sherman-Baust CA;Tsai-Turton M;Bristow RE;Roden RB;Morin PJ
通讯作者:
Morin PJ
影响因子:
16.1
作者:
Butler LM;Perone Y;Dehairs J;Lupien LE;de Laat V;Talebi A;Loda M;Kinlaw WB;Swinnen JV
通讯作者:
Swinnen JV
影响因子:
16
作者:
Ludwig AK;De Miroschedji K;Doeppner TR;Börger V;Ruesing J;Rebmann V;Durst S;Jansen S;Bremer M;Behrmann E;Singer BB;Jastrow H;Kuhlmann JD;El Magraoui F;Meyer HE;Hermann DM;Opalka B;Raunser S;Epple M;Horn PA;Giebel B
通讯作者:
Giebel B
影响因子:
3.7
作者:
Duijvesz D;Burnum-Johnson KE;Gritsenko MA;Hoogland AM;Vredenbregt-van den Berg MS;Willemsen R;Luider T;Paša-Tolić L;Jenster G
通讯作者:
Jenster G