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There is a lower rate of BRAF V600E protein positivity in papillary thyroid carcinoma with comorbid Hashimoto thyroiditis, as well as a higher rate of RET rearrangements positive in papillary thyroid carcinoma with comorbid Hashimoto thyroiditis.

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Targeted Therapeutic Options in Early and Metastatic NSCLC-Overview

Targeted Therapeutic Options in Early and Metastatic NSCLC-Overview

Source : https://www.por-journal.com/articles/10.3389/pore.2024.1611715/full

The complex therapeutic strategy of non-small cell lung cancer (NSCLC) has changed significantly in recent years. Disease-free survival increased significantly with immunotherapy and chemotherapy registered in perioperative treatments, as well...

Incorporating reflex testing with next-generation sequencing expands personalized therapies by identifying guideline-recommended molecular alterations.

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RET Splice Site Variants in Medullary Thyroid Carcinoma

RET Splice Site Variants in Medullary Thyroid Carcinoma

Source : https://pubmed.ncbi.nlm.nih.gov/38566816/

Introduction: Medullary thyroid carcinoma (MTC) is an aggressive cancer that is often caused by driver mutations in RET . Splice site variants (SSV) reflect changes in mRNA processing, which may...

All 25 medullary thyroid carcinoma specimens analyzed had at least one of the 2 most common RET slice site variants, including 4 with no identified mutational driver.

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Developing Dynamic Structure-Based Pharmacophore and ML-Trained QSAR Models for the Discovery of Novel Resistance-Free RET Tyrosine Kinase Inhibitors

Developing Dynamic Structure-Based Pharmacophore and ML-Trained QSAR Models for the Discovery of Novel Resistance-Free RET Tyrosine Kinase Inhibitors

Source : https://pubmed.ncbi.nlm.nih.gov/38523069/

Activation of RET tyrosine kinase plays a critical role in the pathogenesis of various cancers, including non-small cell lung cancer, papillary thyroid cancers, multiple endocrine neoplasia type 2A and 2B...

Extensive small molecule libraries were screened using developed ligand-based models and potent compounds which are capable of inhibiting RET activation were proposed.

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Developing Dynamic Structure-Based Pharmacophore and ML-Trained QSAR Models for the Discovery of Novel Resistance-Free RET Tyrosine Kinase Inhibitors

Developing Dynamic Structure-Based Pharmacophore and ML-Trained QSAR Models for the Discovery of Novel Resistance-Free RET Tyrosine Kinase Inhibitors

Source : https://pubmed.ncbi.nlm.nih.gov/38523069/

Activation of RET tyrosine kinase plays a critical role in the pathogenesis of various cancers, including non-small cell lung cancer, papillary thyroid cancers, multiple endocrine neoplasia type 2A and 2B...

Extensive small molecule libraries were screened using developed ligand-based models and potent compounds which are capable of inhibiting RET activation were proposed.