Small Molecular Inhibitors Reverse Cancer Metastasis by Blockading Oncogenic PITPNM3

Most cancer‐related deaths are a result of metastasis. The development of small molecular inhibitors reversing cancer metastasis represents a promising therapeutic opportunity for cancer patients. This pan‐cancer analysis identifies oncogenic roles of membrane‐associated phosphatidylinositol transfe...

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Veröffentlicht in:Advanced science 2022-12, Vol.9 (35), p.e2204649-n/a
Hauptverfasser: Liu, Zihao, Shi, Yu, Lv, Li, Chen, Jianing, Jiang, WenG, Li, Jun, Lin, Qun, Fang, Xiaolin, Gao, Jingbo, Liu, Yujie, Liu, Qiang, Xu, Xiaoding, Song, Erwei, Gong, Chang
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Sprache:eng
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Zusammenfassung:Most cancer‐related deaths are a result of metastasis. The development of small molecular inhibitors reversing cancer metastasis represents a promising therapeutic opportunity for cancer patients. This pan‐cancer analysis identifies oncogenic roles of membrane‐associated phosphatidylinositol transfer protein 3 (PITPNM3), which is crucial for cancer metastasis. Small molecules targeting PITPNM3 must be explored further. Here, PITPNM3‐selective small molecular inhibitors are reported. These compounds exhibit target‐specific inhibition of PITPNM3 signaling, thereby reducing metastasis of breast cancer cells. Besides, by using nanoparticle‐based delivery systems, these PITPNM3‐selective compounds loaded nanoparticles significantly repress metastasis of breast cancer in mouse xenograft models and organoid models. Notably, the results establish an important metastatic‐promoting role for PITPNM3 and offer PITPNM3 inhibition as a therapeutic strategy in metastatic breast cancer. Pan‐cancer analysis identifies oncogenic roles of membrane‐associated phosphatidylinositol transfer protein 3 (PITPNM3). Small molecule inhibitors targeting PITPNM3 exhibit target‐specific inhibition of PITPNM3 signaling, thereby reducing metastasis of breast cancer. By using nanoparticle‐based delivery systems, PITPNM3‐selective compounds loaded nanoparticles significantly repress metastasis of breast cancer in vivo and in vitro.
ISSN:2198-3844
2198-3844
DOI:10.1002/advs.202204649