My long-term goals are two-fold: 1) to understand the molecular mechanism of prenatal CrVI exposure on placental and fetal development, ovarian and uterine function, and pregnancy outcome, and; 2) to understand the protective effects of various natural and synthetic antioxidants (such as edaravone, glutathione, vitamin C and resveratrol) against the deleterious effects of heavy-metals, CrVI in particular. Current research in my lab is focused on the study of reproductive and developmental toxicity of CrVI. Drinking water contamination with CrVI in the United States is a growing problem due to increased usage of CrVI and improper disposal of Cr waste into the environment. Significant contamination with CrVI has been found in the drinking water sources of all the states in the U.S. Effects of Cr on reproductive health in women and development in children have received less attention. Epidemiological data document that women exposed to Cr in environmental or occupational settings suffer from infertility, gynecological problems, congenital malformation of fetuses, neonatal mortality, and premature abortions with increased levels of Cr in their blood, urine and placenta. Cr can bind directly to DNA and nuclear proteins, cause DNA strand breaks and mutations, alter the balance between reactive oxygen species (ROS) and antioxidants, and activate several cell signaling pathways. Therefore, my current research objective is to determine molecular pathways and identify target genes/proteins by which Cr alters prenatal development and organogenesis of female reproductive system in the offspring.
- Stanley, J. A., Arosh, J. A., Hoyer, P. B., & Banu, S. K. (2019). Ex Vivo Fetal Whole Ovarian Culture Model: An Essential Tool for Studies in Reproductive Toxicology and Pharmacology.. Methods in molecular biology (Clifton, N.J.). 1965, 107-127.
- Banu, S. K. (2018). Chromium Burden in Human Placenta: Author(s) Responses to Thompson et al. Toxicol Sci. 165(2), 270-271.
- Arosh, J. A., & Banu, S. K. (2018). Dual inhibition of ERK1/2 and AKT pathways is required to suppress the growth and survival of endometriotic cells and lesions.. MOLECULAR AND CELLULAR ENDOCRINOLOGY.
- Arosh, J. A., & Banu, S. K. (2018). Molecular, cellular, and epigenetic signatures of prostaglandin E
2in endometriosis. Current Women's Health Reviews. 14(2), 127-146.
- Sales, M. S., Roy, A., Antony, L., Banu, S. K., Jeyaraman, S., & Manikkam, R. (2018). Octyl gallate and gallic acid isolated from Terminalia bellarica regulates normal cell cycle in human breast cancer cell lines. BIOMEDICINE & PHARMACOTHERAPY. 103, 1577-1584.
- Stanley, J. A., Stanley, J. A., Neelamohan, R., Suthagar, E., Annapoorna, K., Sharmila, S., ... Aruldhas, M. M. (2014). Androgen Receptor Expression in Human Thyroid Cancer Tissues: A Potential Mechanism Underlying the Gender Bias in the Incidence of Thyroid Cancers. R. Sudhakaran, P. (Eds.), Perspectives in Cancer Prevention-Translational Cancer Research. (pp. 121-132). Springer India.
- Banu, S. (2013). Heavy Metals and the Ovary. Target Organ Toxicology Series. (pp. 191-228). CRC Press.
- Banu, S. K. (2013). Heavy metals and the ovary. Ovarian Toxicology, Second Edition. (pp. 191-228).
- Banu, S. K., Stanley, J. A., Sivakumar, K. K., & Arosh, J. A. (2017). Exposure to CrVI During Early Pregnancy Increases Oxidative Stress and Disrupts the Expression of Antioxidant Proteins in Placental Compartments.. REPRODUCTIVE SCIENCES. 24, 213A-213A.
- Arosh, J. A., Lee, J., Bruner-Tran, K. L., Osteen, K. G., & Banu, S. K. (2017). Prostaglandin E2 Signaling, Estrogen-Dominance and Progesterone-Resistance in Endometriosis.. REPRODUCTIVE SCIENCES. 24, 59A-59A.
- Arosh, J. A., Lee, J., Meagher, M., Osteen, K., Bruner-Tran, K., & Banu, S. (2013). UNRAVELING THE MOLECULR INTERACTIONS BETWEEN PGE2 SIGNALING AND PAIN PATHWAYS IN ENDOMETRIOSIS. Fertility and Sterility. 100(3), S103-S103.
- Banu, S. K., Lee, J., Burghardt, R. C., & Arosh, J. A. (2012). Combined Inhibition of ERK1/2 and AKT Pathways Induces Apoptosis of Human Endometriotic Epithelial and Stromal Cells through Intrinsic Apoptotic Mechanisms. REPRODUCTIVE SCIENCES. 19(S3), 138A-138A.
- Stanley, J. A., Lee, J., Arosh, J. A., Hoyer, P. B., Burghardt, R. C., & Banu, S. K. (2011). Hexavalent Chromium Through Lactational Exposure Delayed Follicular Development in Pre-Pubertal F1 Offspring: Mechanistic Insights into Cell Cycle Regulation of Granulosa Cells. Biology of Reproduction. 85,