Pyrrolo [2, 1-f][1, 2, 4] triazine: a promising fused heterocycle to target kinases in cancer therapy

S Singh, D Utreja, V Kumar - Medicinal Chemistry Research, 2022 - Springer
Cancer is the second leading cause of death worldwide responsible for about 10 million
deaths per year. To date several approaches have been developed to treat this deadly …

Interleukin-1β induces tissue factor expression in A549 cells via EGFR-dependent and-independent mechanisms

T Mechelke, F Wittig, R Ramer, B Hinz - International journal of molecular …, 2021 - mdpi.com
Tissue factor (TF) plays an important role in the progression and angiogenesis of tumor
cells. The present study investigated the mechanism of interleukin-1β (IL-1β)-induced TF …

[HTML][HTML] Comparison of T790M acquisition between patients treated with afatinib and gefitinib as first-line therapy: retrospective propensity score matching analysis

BW Yoon, JH Kim, SH Lee, CM Choi, JK Rho… - Translational …, 2019 - Elsevier
Afatinib, a second-generation, irreversible pan-HER inhibitor, shows better suppression of
T790M-positive lung cancer cells than gefitinib in preclinical studies. However, whether the …

Design, synthesis, and docking study of new quinoline derivatives as antitumor agents

EE Nasr, AS Mostafa, MAA El‐Sayed… - Archiv der …, 2019 - Wiley Online Library
New quinolines substituted with various heterocycles and chalcone moieties were
synthesized and evaluated as antitumor agents. All the synthesized compounds were in vitro …

[Retracted] The Use of Cytotoxic Drugs as First Line Chemotherapy for EGFR (+) Nonsquamous NSCLC: A Network Meta‐Analysis

D Li, M Li, H Li, P Shi, M Chen, T Yang - Disease Markers, 2023 - Wiley Online Library
Objective. To assess the use of cytotoxic drugs as first‐line chemotherapy for nonsquamous
non‐small‐cell lung cancer (NSCLC) with EGFR mutation. Method. This study uses the …

Design, synthesis and bioactivity evaluation of the combination of evodiamine and erlotinib linked by indolequinone

B Wei, J Ma, H Guo, Y Wang, D Guo, Y Tang - Bioorganic & Medicinal …, 2024 - Elsevier
Compared with single-targeted therapy, the design and synthesis of heterozygous
molecules is still a significant challenge for the discovery of antitumor drugs. Quinone …

Review of Personalized Medicine and Pharmacogenomics of Anti-Cancer Compounds and Natural Products

Y Zhou, S Peng, H Wang, X Cai, Q Wang - Genes, 2024 - mdpi.com
In recent years, the FDA has approved numerous anti-cancer drugs that are mutation-based
for clinical use. These drugs have improved the precision of treatment and reduced adverse …

Potential use of EGFR-targeted molecular therapies for tumor suppressor CYLD-negative and poor prognosis oral squamous cell carcinoma with chemoresistance

A Kanemaru, S Shinriki, M Kai, K Tsurekawa… - Cancer Cell …, 2022 - Springer
Background Tumor suppressor CYLD dysfunction by loss of its expression, triggers
malignant transformation, especially drug resistance and tumor invasion/metastasis …

Follicle stimulating hormone controls granulosa cell glutamine synthesis to regulate ovulation

KH Zhang, FF Zhang, ZL Zhang, KF Fang… - Protein & …, 2024 - academic.oup.com
Polycystic ovary syndrome (PCOS) is the leading cause of anovulatory infertility. Inadequate
understanding of the ovulation drivers hinders PCOS intervention. Herein, we report that …

[HTML][HTML] Comparison of effectiveness of Gefitinib, Erlotinib, and Afatinib in advanced non-small cell lung cancer patients with EGFR mutation positive in Indonesian …

N Sutandyo, A Hanafi, M Jayusman - Chinese journal of lung …, 2019 - ncbi.nlm.nih.gov
Methods A retrospective cohort study of 88 NSCLC patients with EGFR mutation positive
treated with gefitinib (n= 59), erlotinib (n= 22), and afatinib (n= 7) was performed in national …