Notably, in vitro functional assays of the less-reported gene SLC19A1 demonstrated its role in promoting LARC progression. This study offers new insights into the molecular mechanisms underlying LARC pathogenesis and identifies potential therapeutic targets.
An eight-gene CSC signature captures a stemness-linked G2/M program that generalizes across cohorts, relates to the microenvironment, and is therapeutically tractable via kinase targeting, providing a compact readout for risk stratification and preclinical screening.
3 days ago
Journal
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TOP2A (DNA topoisomerase 2-alpha) • AURKA (Aurora kinase A) • PLK1 (Polo Like Kinase 1) • CDCA8 (Cell Division Cycle Associated 8) • KIF23 (Kinesin Family Member 23)
Genes such as SYP show significant differential expression in both T2DM and RC and may play significant roles in the progression of T2DM and RC. Transcription factor analysis suggested that SP1 could regulate multiple hub genes. Molecular docking indicated that SP1 is a potential target for active components like stearic acid and EGCG in Ginkgo biloba, highlighting its potential as a therapeutic agent for T2DM and RC.
3 days ago
Journal
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ER (Estrogen receptor) • CDH3 (Cadherin 3) • SYP (Synaptophysin) • CHGA (Chromogranin A)
P=N/A, N=30, Recruiting, University of South Florida | Trial completion date: Jun 2025 --> Jun 2027 | Trial primary completion date: Dec 2024 --> Dec 2026
3 days ago
Trial completion date • Trial primary completion date
The observed toxicity was consistent with the known toxicity profile of immunotherapy and did not lead to discontinuation of therapy. Our case report highlights the need to test for predictive markers in patients with locoregionally advanced rectal cancer in order to identify specific subtypes of the disease that can be treated with immunotherapy with a high probability of achieving clinical complete remission, thereby avoiding potentially risky surgery.
P2, N=38, Suspended, Rutgers, The State University of New Jersey | Trial completion date: Jan 2026 --> Jan 2028 | Recruiting --> Suspended | Trial primary completion date: Jan 2026 --> Dec 2027
9 days ago
Trial completion date • Trial suspension • Trial primary completion date
All enrolled patients received conventional radiotherapy combined with CapeOX or capecitabine monotherapy, along with serplulimab, followed by TME 8-12 weeks post-nCRT. The combination of serplulimab with nCRT demonstrated safety and efficacy in patients with high-risk pMMR LARC. However, further verification through longer follow-up periods and large-scale prospective studies is warranted.