Moreover, the functional mechanisms by which circRNAs contribute to GC pathogenesis and therapeutic resistance warrant further investigation. Advances in circRNAs research could provide valuable insights into the early detection and targeted treatment of GC, ultimately improving patient outcomes.
Furthermore, adenoviral therapy targeting Shkbp1 indicated that knockout of Shkbp1 increased CD8 + T cells and inhibited tumor growth. This study provides new insights into the role of Shkbp1 in CD8 differentiation and functions, suggesting that Shkbp1 may be a new, potential target in cancer immunotherapy.
over 2 years ago
Preclinical • Journal
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CD8 (cluster of differentiation 8) • SHKBP1 (SH3KBP1 Binding Protein 1)
All data including HR and p values as well as the used cutoff values for all genes for both PFS and OS are provided to enable the ranking of future biomarker candidates across all genes. Our results help to prioritize genes and to neglect those which are most likely to fail in studies aiming to establish new clinically useful biomarkers and therapeutic targets in serous ovarian cancer.
almost 3 years ago
Journal
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ALPK2 (Alpha Kinase 2) • SHKBP1 (SH3KBP1 Binding Protein 1)
Moreover, miR-766-5p inhibition and overexpression of HMGA2 rescued the tumor-suppressing roles of circSHKBP1 downregulation in LSCC. In conclusion, circSHKBP1 accelerated the tumorigenesis of LSCC via modulating HMGA2 by targeting miR-766-5p.
almost 4 years ago
Journal
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HMGA2 (High mobility group AT-hook 2) • SHKBP1 (SH3KBP1 Binding Protein 1)
Seventy-two patients from 16 institutions were enrolled and treated with a TKI, nilotinib...In conclusion, we found that rapidity of response to TKI was associated with pathway-associated genetic alterations in immune cells, particularly with respect to NK cell activity. These results suggested that the innate immune system at initial diagnosis had an important role in treatment response in patients with CML.
almost 4 years ago
Journal
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ABL1 (ABL proto-oncogene 1) • PTPRC (Protein Tyrosine Phosphatase Receptor Type C) • CD2 (CD2 Molecule) • ARHGEF11 (Rho Guanine Nucleotide Exchange Factor 11) • BLNK (B Cell Linker) • GPR183 (G Protein-Coupled Receptor 183) • PTPRCAP (Protein Tyrosine Phosphatase Receptor Type C Associated Protein) • SHKBP1 (SH3KBP1 Binding Protein 1) • TRPV2 (Transient Receptor Potential Cation Channel Subfamily V Member 2)
Thus, exosomal circSHKBP1 participated in the progression of NSCLC via the miR-1294/PKM2 axis. circSHKBP1 may be potential biomarker for the diagnosis and treatment of NSCLC.