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Haiou Yang

Researcher at Tianjin Medical University Cancer Institute and Hospital

Publications -  16
Citations -  1844

Haiou Yang is an academic researcher from Tianjin Medical University Cancer Institute and Hospital. The author has contributed to research in topics: Microvesicles & Cancer. The author has an hindex of 12, co-authored 16 publications receiving 937 citations.

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CAF secreted miR-522 suppresses ferroptosis and promotes acquired chemo-resistance in gastric cancer.

TL;DR: It is demonstrated that CAFs secrete exosomal miR-522 to inhibit ferroptosis in cancer cells by targeting ALOX15 and blocking lipid-ROS accumulation, which results in decreased chemo-sensitivity.
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Exosome-delivered EGFR regulates liver microenvironment to promote gastric cancer liver metastasis

TL;DR: It is proposed that EGFR-containing exosomes derived from cancer cells could favour the development of a liver-like microenvironment promoting liver-specific metastasis and be incorporated on the plasma membrane of liver stromal cells.
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Exosome-delivered circRNA promotes glycolysis to induce chemoresistance through the miR-122-PKM2 axis in colorectal cancer.

TL;DR: In vitro and in vivo studies showed that exosomes from oxaliplatin‐resistant cells delivered ciRS‐122 to sensitive cells, thereby promoting glycolysis and drug resistance through miR‐122 sponging and PKM2 upregulation and establishing a foundation for future clinical applications in drug‐resistant CRC.
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Exosomal circRNA derived from gastric tumor promotes white adipose browning by targeting the miR-133/PRDM16 pathway.

TL;DR: It is shown thatcircRNAs in plasma exosomes have specific expression features in gastric cancer (GC), and ciRS‐133 is linked with the browning of white adipose tissue (WAT) in GC patients, and exosome‐delivered circRNAs are involved in WAT browning and play a key role in cancer‐associated cachexia.
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Exosome-Derived miR-130a Activates Angiogenesis in Gastric Cancer by Targeting C-MYB in Vascular Endothelial Cells.

TL;DR: It is demonstrated that exosomes delivered miR-130a from gastric cancer cells into vascular cells to promote angiogenesis and tumor growth by targeting c-MYB both in vivo and in–vitro.