期刊
ONCOTARGET
卷 8, 期 2, 页码 2681-2693出版社
IMPACT JOURNALS LLC
DOI: 10.18632/oncotarget.13153
关键词
proteome microarray; 6-O-angeloylplenolin; STAT3 inhibitor; Skp2; lung cancer
资金
- National Natural Science Funds for Distinguished Young Scholar [81425025]
- National Key Research and Development Program of China [2016YFC0905500]
- National Natural Science Foundation of China [81672765, 81171925, 81201537]
- State Key Laboratory of Medical Genomics
The S phase kinase- associated protein 1 (Skp1), an adaptor protein of the Skp1-Cul1-F-box protein complex, binds the ubiquitin E3 ligase Skp2 and is critical to its biological functions. Targeting of Skp1 by a small compound 6-O-angeloylplenolin (6-OAP) results in dissociation and degradation of Skp2 and mitotic arrest of lung cancer cells. Here, by using a proteome microarray containing 16,368 proteins and a biotinylated 6-OAP, we identified 99 proteins that could bind 6-OAP, with Skp1 and STAT3 sitting at the central position of the 6-OAP interactome. 6-OAP formed hydrogen bonds with Ser611/Ser613/Arg609 at the SH2 domain of STAT3 and inhibited the constitutive and interleukin-6-induced phosphorylated STAT3 (pSTAT3), leading to inhibitory effects on lung cancer cells and suppression of Skp2 transcription. STAT3 was overexpressed in tumor samples compared to counterpart normal lung tissues and was inversely associated with prognosis of the patients. 6-OAP inhibited tumor growth in SCID mice intravenously injected with lung cancer cells, and downregulated both STAT3 and Skp2 in tumor samples. Given that 6-OAP is a Skp1 inhibitor, our data suggest that this compound may target Skp1 and STAT3 to suppress Skp2, augmenting its anti-lung cancer activity.
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