Consistent with the findings in our study, low expression of RRM1, CYP2W1 and SOAT1 was associated with worse DFS with antitumor therapy. The results of the work indicate the need to assess the levels of immunoreactivity of these markers in patients with ACC before starting treatment with mitotane in order to predict the efficiency of therapy.
almost 2 years ago
Journal
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RRM1 (Ribonucleotide Reductase Catalytic Subunit M1) • CYP2W1 (Cytochrome P450 Family 2 Subfamily W Member 1)
SRRM1 played a significant role in the proliferation, migration, invasion and apoptosis of HCC, and promoted cancer by regulating the JAK/STAT signaling pathway.
The control group randomly received chemotherapy with gemcitabine plus cisplatin or paclitaxel plus cisplatin. The selection of chemotherapy regimen based on mRNA expression of the RRM1, TUBB3, and ERCC1 genes may improve selection of candidate patients to receive clinical chemotherapy. However, large-scale prospective clinical studies are needed for in-depth investigation.
3 years ago
Clinical • Journal
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ERCC1 (Excision repair cross-complementation group 1) • TUBB3 (Tubulin beta 3 class III) • RRM1 (Ribonucleotide Reductase Catalytic Subunit M1)
Our study demonstrated that high RRM1 expression may serve as a poor prognostic biomarker in BLCA patients. Moreover, our study suggested that BLCA patients with high RRM1 expression may benefit more from ICIs therapies than those with low RRM1 expression.