Mohammad Athar

ORCID: 0000-0001-5829-7992
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About
Contact & Profiles
Research Areas
  • Retinoids in leukemia and cellular processes
  • Skin Protection and Aging
  • Legume Nitrogen Fixing Symbiosis
  • melanin and skin pigmentation
  • Agronomic Practices and Intercropping Systems
  • Cancer-related Molecular Pathways
  • Photodynamic Therapy Research Studies
  • Vitamin C and Antioxidants Research
  • Genomics, phytochemicals, and oxidative stress
  • PI3K/AKT/mTOR signaling in cancer
  • Estrogen and related hormone effects
  • Hidradenitis Suppurativa and Treatments
  • Pesticide Exposure and Toxicity
  • Glutathione Transferases and Polymorphisms
  • Carcinogens and Genotoxicity Assessment
  • Antioxidant Activity and Oxidative Stress
  • Cancer Research and Treatments
  • Heavy Metal Exposure and Toxicity
  • Inflammatory mediators and NSAID effects
  • Agricultural Science and Fertilization
  • Nonmelanoma Skin Cancer Studies
  • Colorectal and Anal Carcinomas
  • Phytochemicals and Antioxidant Activities
  • Sulfur Compounds in Biology
  • Arsenic contamination and mitigation

University of Alabama at Birmingham
2016-2025

Birmingham VA Medical Center
2013-2025

Indian Agricultural Research Institute
2023

PricewaterhouseCoopers (South Korea)
2022

Jawaharlal Institute of Post Graduate Medical Education and Research
2022

Aligarh Muslim University
2022

University of Alabama
2011-2021

California Department of Food and Agriculture
2011-2020

University of Karachi
2013-2020

Instituto de Salud Carlos III
2018

Cancer genomic, transcriptomic, and proteomic profiling has generated extensive data that necessitate the development of tools for its analysis dissemination. We developed UALCAN to provide a portal easy exploring, analyzing, visualizing these data, allowing users integrate better understand gene, proteins, pathways perturbed in cancer make discoveries. web enables analyzing delivering transcriptome, proteomics, patient survival research community. With obtained from The Genome Atlas (TCGA)...

10.1016/j.neo.2022.01.001 article EN cc-by-nc-nd Neoplasia 2022-01-22

Glutathione (GSH) plays several important roles in the protection of cells against oxidative damage, particularly following exposure to xenobiotics. Ferric nitrilotriacetate (Fe-NTA) is a potent depletor GSH and also enhances tissue lipid peroxidation. In this study, we show effect Fe-NTA treatment on hepatic some glutathione metabolizing enzymes, oxidant generation liver damage. The level activities reductase, S-transferase, peroxidase, glucose 6-phosphate dehydrogenase all decrease...

10.1080/13510002.1996.11747079 article EN Redox Report 1996-12-01

Abstract The present study was designed to investigate the protective efficacy of eugenol against skin cancer and probe into mechanistic aspects. Skin tumors were initiated by applying 160 nmol DMBA promoted twice weekly applications 8.5 TPA for 28 wk. All mice developed 13 wk promotion. However, in pretreated with 30 µL eugenol, no detected until 8 (following anti‐initiation protocol) 14 antipromotion tumor PCNA TUNEL immunohistochemistry revealed ameliorate cell proliferation elevate...

10.1002/mc.20601 article EN Molecular Carcinogenesis 2009-12-30

Malignant melanoma is responsible for approximately 75% of skin cancer-related deaths. BRAF plays an important role in regulating the mitogen-activated protein kinase (MAPK) signaling cascade with activating mutations serine/threonine occurring 60-70% malignant melanomas. The BRAF-MEK-ERK pathway a key regulator cell invasion. In addition, activation NFκB via MAPK regulated through MEK-induced IKK. These pathways are potential targets prevention and treatment melanoma. this study, we...

10.1371/journal.pone.0086338 article EN cc-by PLoS ONE 2014-01-23

Idiopathic pulmonary fibrosis (IPF) is a progressive disease, with median survival of 3–5 years following diagnosis. Lung remodeling by invasive fibroblasts hallmark IPF. In this study, we demonstrate that inhibition vimentin intermediate filaments (VimIFs) decreases the invasiveness IPF and confers protection against in murine model experimental lung injury. Increased expression organization VimIFs contribute to property connection deficient cellular autophagy. Blocking VimIF assembly...

10.1172/jci.insight.123253 article EN JCI Insight 2019-04-03

Inflammatory stimuli result in the production of cutaneous eicosanoids, which are known to contribute process tumor promotion. Cyclooxygenase (COX), rate-limiting enzyme for prostaglandins (PG) from arachidonic acid, exists at least two isoforms, COX-1 and COX-2. is constitutively expressed most tissues plays various physiological roles, whereas increased COX-2 expression occur several types epithelial neoplasms. Enhanced PG synthesis a potential contributing factor UVB-induced nonmelanoma...

10.1562/0031-8655(2002)076<0073:ceimah>2.0.co;2 article EN Photochemistry and Photobiology 2002-01-01

Ferric nitrilotriacetate (Fe-NTA) is a known complete renal carcinogen. In this study we show that Fe-NTA potent inducer of ornithine decarboxylase (ODC) activity and DNA synthesis promoter N-diethylnitrosamine (DEN)-induced tumorigenesis in rat. induced ODC several fold as compared with saline-treated rats. Renal synthesis, measured [3H]thymidine incorporation into DNA, was increased after treatment. Similar to other tumor promoters, also depleted the antioxidant armory tissue. It...

10.1093/carcin/19.6.1133 article EN Carcinogenesis 1998-06-01

Mutations in the tumor suppressor p53 are detectable over 50% of all human malignancies. Mutant protein is incapable transactivating its downstream target genes that required for DNA repair and apoptosis. Chronic exposure to UVB induces mutations carcinogenic both murine skin. CP-31398, a styrylquinazoline compound, restores functions mutant forms cells. However, effectiveness vivo remains unclear. Here, we demonstrate CP-31398 blocked UVB-induced skin carcinogenesis was associated with...

10.1172/jci32481 article EN Journal of Clinical Investigation 2007-12-03
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