Title : The BAFF/NFκB axis is crucial to interactions between sorafenib-resistant HCC cells and cancer-associated fibroblasts.

Pub. Date : 2021 Sep

PMID : 34159680






5 Functional Relationships(s)
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1 We established a sorafenib-resistant Huh7 (human HCC) cell line, and characterized it with cytokine assays, then developed CAFs by co-culturing human hepatic stellate cells with resistant or parental Huh7 cells. Sorafenib MIR7-3 host gene Homo sapiens
2 The sorafenib-resistant Huh7 (Huh7SR ) cells expressed increased B-cell activating factor (BAFF), which promoted highly expression of CAF specific markers in Huh7SR -co-cultured CAFs, showed activated BAFF, BAFF-R and downstream NFkappaB-Nrf2 pathway, and aggravated invasion, migration and drug resistance in co-cultured Huh7 cells. Sorafenib MIR7-3 host gene Homo sapiens
3 The sorafenib-resistant Huh7 (Huh7SR ) cells expressed increased B-cell activating factor (BAFF), which promoted highly expression of CAF specific markers in Huh7SR -co-cultured CAFs, showed activated BAFF, BAFF-R and downstream NFkappaB-Nrf2 pathway, and aggravated invasion, migration and drug resistance in co-cultured Huh7 cells. Sorafenib MIR7-3 host gene Homo sapiens
4 The sorafenib-resistant Huh7 (Huh7SR ) cells expressed increased B-cell activating factor (BAFF), which promoted highly expression of CAF specific markers in Huh7SR -co-cultured CAFs, showed activated BAFF, BAFF-R and downstream NFkappaB-Nrf2 pathway, and aggravated invasion, migration and drug resistance in co-cultured Huh7 cells. Sorafenib MIR7-3 host gene Homo sapiens
5 The sorafenib-resistant Huh7 (Huh7SR ) cells expressed increased B-cell activating factor (BAFF), which promoted highly expression of CAF specific markers in Huh7SR -co-cultured CAFs, showed activated BAFF, BAFF-R and downstream NFkappaB-Nrf2 pathway, and aggravated invasion, migration and drug resistance in co-cultured Huh7 cells. Sorafenib MIR7-3 host gene Homo sapiens