EphA2 in Cancer: Molecular Complexity and Therapeutic Opportunities DOI Open Access
Lisa Toracchio, Marianna Carrabotta, Caterina Mancarella

et al.

International Journal of Molecular Sciences, Journal Year: 2024, Volume and Issue: 25(22), P. 12191 - 12191

Published: Nov. 13, 2024

Erythropoietin-producing hepatocellular A2 (EphA2) is a member of the Eph tyrosine kinase receptor family that has been linked to various biological processes. In tumors, EphA2 overexpression associated with noncanonical pathway activation, tumor progression, and poor prognosis, which emphasized its importance as marker malignancy. Studies on numerous cancer models have highlighted EphA2’s dual often contradictory action, can be attributed EphA2′s interactions involving multiple pathways different ligands, well heterogeneity microenvironment. this review, we summarize main mechanisms underlying dysregulation in cancer, highlighting molecular complexity. Then, analyze therapies developed over time counteract action. We discuss limitations described approaches, emphasizing fact goal new options high specificity without losing therapeutic efficacy. For reason, immunotherapy or emerging field targeted protein degradation proteolysis-targeting chimeras (PROTACs) may represent promising solution based deeper understanding sustaining oncogenic activity.

Language: Английский

Association between pan-immune-inflammation value and heart failure: Evidence from the NHANES 2011–2020 DOI Creative Commons
Chen Fu, Yijie Mao

Journal of International Medical Research, Journal Year: 2025, Volume and Issue: 53(3)

Published: March 1, 2025

Objective This study aimed to explore the association between pan-immune-inflammation value and heart failure outcomes using data from nationally representative National Health Nutrition Examination Survey database. Methods We conduct a cross-sectional cohort analysis data, including participants aged ≥20 years with available data. performed smooth curve fitting threshold analysis, both linear non-linear regression models, assess dose–response relationship continuous effect of on outcomes. Results Our revealed significant independent elevated levels an increased risk occurrence. After adjustment for multiple covariates, these findings remained consistent each increment unit in logarithmic is associated 34% increase Furthermore, we identified inflection point = 5.98 as critical threshold. Stratified analyses that occurrence remains across different subgroups. Conclusions confirmed clinical novel inflammatory biomarker assessment monitoring failure.

Language: Английский

Citations

0

Oral selective estrogen receptor degraders (SERDs) in Hormone receptor-Positive HER2-Negative Metastatic breast cancer After Progression with CDK4/6 inhibitors DOI
Taha Koray Şahin, Sercan Aksoy, Deniz Can Güven

et al.

Expert Review of Anticancer Therapy, Journal Year: 2025, Volume and Issue: unknown

Published: March 13, 2025

Hormone receptor-positive (HR+), HER2-negative metastatic breast cancer (mBC) remains a prevalent and challenging disease. Endocrine therapy (ET) combined with CDK4/6 inhibitors is the first-line standard of care, yet resistance mechanisms, including ESR1 mutations, drive disease progression. Novel oral selective estrogen receptor degraders (SERDs) have emerged as promising therapeutic agents after progression secondary to mutations. However, available studies on SERDs differ in design, study population, outcomes, necessitating critical review data. This explores clinical efficacy, safety profiles HR-positive, mBC, particularly following inhibitors. Recent key trials, EMERALD, SERENA-2, EMBER-3 AMEERA-3, are analyzed, highlighting their efficacy overcoming resistance, especially ESR1-mutant populations. Oral offer enhanced bioavailability convenience compared fulvestrant, representing advancement endocrine therapy. Their integration into treatment strategies, combination regimens ctDNA-driven approaches, may improve patient outcomes address mechanisms. other than refinement for selection limited. Further trials needed optimize SERD use define most effective strategies SERDs.

Language: Английский

Citations

0

EphA2 in Cancer: Molecular Complexity and Therapeutic Opportunities DOI Open Access
Lisa Toracchio, Marianna Carrabotta, Caterina Mancarella

et al.

International Journal of Molecular Sciences, Journal Year: 2024, Volume and Issue: 25(22), P. 12191 - 12191

Published: Nov. 13, 2024

Erythropoietin-producing hepatocellular A2 (EphA2) is a member of the Eph tyrosine kinase receptor family that has been linked to various biological processes. In tumors, EphA2 overexpression associated with noncanonical pathway activation, tumor progression, and poor prognosis, which emphasized its importance as marker malignancy. Studies on numerous cancer models have highlighted EphA2’s dual often contradictory action, can be attributed EphA2′s interactions involving multiple pathways different ligands, well heterogeneity microenvironment. this review, we summarize main mechanisms underlying dysregulation in cancer, highlighting molecular complexity. Then, analyze therapies developed over time counteract action. We discuss limitations described approaches, emphasizing fact goal new options high specificity without losing therapeutic efficacy. For reason, immunotherapy or emerging field targeted protein degradation proteolysis-targeting chimeras (PROTACs) may represent promising solution based deeper understanding sustaining oncogenic activity.

Language: Английский

Citations

1