This combination treatment mitigated MPTT-induced PD-L1 upregulation and alleviated T cell exhaustion. Collectively, these findings demonstrate a synergistic strategy that enhances photothermal immunotherapy through the co-delivery of siRNA and miRNA to suppress PD-L1, enabling potent and systemic antitumor responses.
In vivo experiments further demonstrated that silencing TMPO-AS1 inhibited tumor growth. This study unveils a novel TMPO-AS1/miR-140-5p/DNMT1/KLK10 regulatory axis that plays a critical role in cisplatin resistance in CC, providing a potential therapeutic target for overcoming chemoresistance.
Furthermore, we identify methyltransferase-like 3 (METTL3)-dependent m6A modification as a critical regulator of circIST1 stability. Collectively, our findings uncover a novel m6A-circIST1-miR-140-3p/miR-182-HIF-1α regulatory axis that underlies metabolic reprogramming in HCC, positioning circIST1 as a promising therapeutic target for HCC metabolic intervention.
ORC1 represents a promising therapeutic target, as its inhibition induces replication stress, cell cycle arrest, and enhances sensitivity to existing chemotherapeutic agents. Future research should focus on developing specific ORC1 inhibitors and exploring their synergistic potential with immunotherapy and targeted therapies.
2 months ago
Review • Journal • IO biomarker
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IGF2BP1 (Insulin Like Growth Factor 2 MRNA Binding Protein 1) • SLC7A11 (Solute Carrier Family 7 Member 11) • ETV4 (ETS Variant Transcription Factor 4) • MIR140 (MicroRNA 140) • ORC1 (Origin Recognition Complex Subunit 1) • XIST (X Inactive Specific Transcript)
Collectively, these findings demonstrate that distinct miRNA profiles can differentiate pediatric sarcoma types and subtypes and offer clinically relevant insights into tumor biology, prognosis, and potential diagnostic application.
Notably, saliva emerged as the most promising biofluid for GC diagnosis, achieving superior receiver-operating characteristic curve values compared with plasma and tissue. This study highlights the role of BEST and MBA in advancing single-EVP analysis and elucidating EVP trafficking, paving the way for future diagnostic applications of EVP cargo.
A nomogram integrating CKS1B expression with clinical parameters effectively predicted 3- and 5-year survival probabilities, offering a tool for personalized risk assessment. In conclusion, our findings position CKS1B as a key factor in LUAD progression and suggest that targeting MAPK/ERK signaling could enhance the efficacy of immunotherapy and overcome chemoresistance.
Moreover, SUZ12 polycomb repressive complex 2 subunit (SUZ12) was directly targeted by miR-140-3p, overexpression or inhibition of SUZ12 in AML cells partially counteracted miR-140-3p agomir or antagomir-mediated cellular effects, respectively. Our study suggested that the BMSCs-derived exosomal miR-140-3p, rather than miR-142-5p and miR-142-3p, has a regulatory effect on the growth and apoptosis of AML cells by targeting SUZ12.
In addition, SRSF10 is a downstream binding target of miR-140-3p, and inhibition of SRSF10 also promoted pyroptosis and inhibited glioma cells proliferation and metastasis. In conclusion, our results confirmed that PSMA1-AS1 affects glioma cell proliferation and metastasis by regulating pyroptosis through miR-140-3p/SRSF10 axis, suggesting that LncRNA PSMA1-AS1 may be a potential target for glioma.
The histopathological assessment of myocardial damage provided supportive evidence for the biochemical results obtained. In conclusion, the BB extract (80.0 mg/kg) can attenuate the DOX-induced oxidative stress, and it has the potential to be developed as an adjunct against DOX-induced cardiotoxicity in cancer patients who undergo anthracycline chemotherapy.
Selected lncRNAs, including THOR and LINC01094, have also demonstrated significant prognostic value. Despite these advances, challenges persist, including inconsistent reporting, limited external validation, and a lack of replication by independent research groups.
This case-control study, aimed to evaluate the expression profiles of specific microRNAs (miRNAs)-miR-155-5p, miR-21-5p, miR-93-5p, and miR-140-5p-in 50 female BC patients treated with paclitaxel (PTX) compared to 50 healthy controls...The findings underscore the importance of miRNAs in BC biology and their potential to guide personalized therapeutic strategies. Validation in larger cohorts is recommending and exploring miRNA-based interventions to improve patient outcomes and overcome chemoresistance in BC.