Publications by authors named "V S Gawali"

Article Synopsis
  • AM-101, a synthetic drug that activates GABA(A) receptors, shows promise in treating non-small cell lung cancer (NSCLC) by reducing cell viability and enhancing the efficacy of radiation therapy.
  • The drug has comparable effectiveness to docetaxel, a common chemotherapy, in both laboratory and living models, particularly benefitting mice with brain metastases.
  • Activation of the GABA(A) receptor triggers a specific autophagic process that helps improve tumor control and could allow for lower radiation doses, potentially reducing side effects for patients.
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Rheumatoid arthritis (RA) is a chronic inflammatory autoimmune disease that affects the synovial joint, which leads to inflammation, loss of function, joint destruction, and disability. The disease biology of RA involves complex interactions between genetic and environmental factors and is strongly associated with various immune cells, and each of the cell types contributes differently to disease pathogenesis. Several immunomodulatory molecules, such as cytokines, are secreted from the immune cells and intervene in the pathogenesis of RA.

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Unlabelled: In non-small cell lung cancer (NSCLC) treatment, targeted therapies benefit only a subset of NSCLC, while radiotherapy responses are not durable and toxicity limits therapy. We find that a GABA(A) receptor activator, AM-101, impairs viability and clonogenicity of NSCLC primary and brain metastatic cells. Employing an 'chip', AM-101 is as efficacious as the chemotherapeutic docetaxel, which is used with radiotherapy for advanced-stage NSCLC.

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Ion channels are critical for cell development and maintaining cell homeostasis. The perturbation of ion channel function contributes to the development of a broad range of disorders or channelopathies. Cancer cells utilize ion channels to drive their own development, as well as to improve as a tumor and to assimilate in a microenvironment that includes various non-cancerous cells.

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