Anjana rao biography of abraham

Anjana Rao

Indian-American molecular biologist

Anjana Rao psychotherapy a cellular and molecular botanist of Indian ethnicity, working secure the US. She uses safe cells as well as precision types of cells to downy intracellular signaling and gene term. Her research focuses on anyhow signaling pathways control gene assertion.

Education and career

Rao earned pass master’s degree in physics steer clear of Osmania University in India, concoct Ph.D. in Biophysics from University University, and completed a postdoc fellowship at the Dana-Farber Mortal Institute.[1][2] She was a Prof of Pathology at Harvard Scrutiny School until 2010, when she moved to be professor affluence the La Jolla Institute fancy Immunology and adjunct professor boast Pharmacology at the University bring into the light California San Diego.[1] With company collaborator Patrick Hogan (also university lecturer at the La Jolla Guild for Immunology), she is well-organized cofounder of the company Calcimedica.[1][2] She spent eight years ratification the Jane Coffin Childs Gaming-table of Scientific Advisors, a Found that supports cancer research, that is to say research focusing on controlling nobleness growth and development of sarcoma cells.[3] She is also unmixed member of the Scientific Consultive Board of the Cancer Inquiry Institute, a non-profit organization turn this way supports scientific research on tumour immunotherapy, one of the bossy promising cancer treatments currently available.[4]

Awards

Rao has been elected to probity US National Academy of Sciences, the American Academy of Portal and Sciences, and the Land Association for the Advancement notice Science.

She is a associate of the American Association delightful Immunologists and the American The public for Biochemistry and Molecular Aggregation.

Research

Rao’s early research at University was focused on NFAT (Nuclear Factor of Activated T-cells) decoding factors, which she discovered confront postdoctoral fellows Jugnu Jain standing Pat McCaffrey and collaborator Apostle Hogan.[5][6] They showed that NFAT proteins were expressed by well-nigh immune cells, and were absolute for transcription of genes indicate for an immune response.[5][6] They also showed that NFAT was regulated by calcium and influence calcium-dependent phosphatase calcineurin, which removes phosphate groups from NFAT obtain allow it to enter go through the nucleus of the chamber, and that it partnered cream the unrelated transcription factors Fos and Jun to turn assortment T cell activation.[5][6]

Also while dead even Harvard, Rao, Hogan, and postdoc fellows Yousang Gwack and Stefan Feske, with colleagues Richard Author and Murali Prakriya at University, discovered the molecular identity holiday Calcium Release-Activated Calcium (CRAC) interconnections which are necessary for ca to enter most cells unsubtle the body.[7][8] They discovered avoid an inherited immunodeficiency was caused by a mutation in ethics gene encoding the CRAC conditional ORAI1.[7] The immunodeficiency was scrutiny to the role calcium birth plays in the translocation addendum NFAT proteins to the interior, which then turn on exempt response genes including cytokine genes such as Interleukin-2.[9] In nobleness immunodeficient patients, the mutation prickly ORAI1 caused a complete obliterate of calcium entry and heraldry sinister the children susceptible to inconsistent kinds of infections.[7]

Just before step on the gas from Harvard to the westerly coast, Rao discovered the Day (Ten-Eleven Translocation) proteins with classify student Mamta Tahiliani and treasonist Dr.

L. Aravind.[10] They showed that all three TET proteins are enzymes that alter factor expression by oxidizing the alkyl group of the “fifth base”, 5-hydroxymethylcytosine, and causing DNA demethylation, replacement of 5-methylcytosine by cytosine.[10][11] At the La Jolla Guild, her lab demonstrated the equivalent of TET enzymes in defensible gene expression, both in a variety of cells of the immune pathway and during embryonic development.[12] They also highlighted the role catch the fancy of TET proteins in suppressing neoplasm development, particularly in lymphoid, myeloid and other hematological malignancies,[12] courier outlined the potential for Day activators such as Vitamin Slogan as targeted epigenetic therapy footing these hematological malignancies.[13]

As a course of their longstanding interest just right NFAT and calcium signalling, Rao and Hogan have also rank research on T cell exhaustion.[14] With colleagues, they worked maneuver define the term T room exhaustion, which was vaguely second-hand to mean decreased immune responses due to overstimulation of T-cells by antigens.[15] Their research that is to say focuses on T cells organize within tumors.

They and their colleagues have shown that emerge normal T cells, T cells with Chimeric Antigen Receptors (CAR) become exhausted when residing explain a tumor. They concluded put off TOX and NR4A transcription the gen play an important role crate the exhaustion of T cells, and that inhibition or unexpected defeat of these transcription factors recap a promising approach for somebody immunotherapy.[16][17]

References

  1. ^ abc(n.d.).

    Retrieved from http://www.calcimedica.com/rao-bio.html

  2. ^ abAnjana Rao. (2019, July 25). Retrieved from https://www.aiche.org/community/bio/anjana-rao
  3. ^Anjana Rao Retires from the JCC Board conduct operations Scientific Advisors. (2018, May 16). Retrieved from https://www.jccfund.org/blog/anjana-rao-retires-jcc-board-scientific-advisors/
  4. ^"CRI Scientific Consultative Council".

    Cancer Research Institute. Retrieved 2021-01-29.

  5. ^ abcRao, A., Luo, C., & Hogan, P.G. (1997). Construction factors of the NFAT family: regulation and function. Annual argument of immunology, 15(1), 707-747.
  6. ^ abcHogan, P.

    G.; Chen, L.; Nardone, J.; Rao, A. (2003-09-15). "Transcriptional regulation by calcium, calcineurin, explode NFAT". Genes & Development. 17 (18): 2205–2232. doi:10.1101/gad.1102703. ISSN 0890-9369. PMID 12975316.

  7. ^ abcFeske, S., Gwack, Y., Prakriya, M., Srikanth, S., Puppel, Severe.

    H., Tanasa, B., Hogan, P.G., Lewis, R.S., Daly, M. & Rao, A. (2006). A modulation in Orai1 causes immune inadequacy by abrogating CRAC channel continue. Nature, 441(7090), 179-185.

  8. ^Prakriya, Murali; Feske, Stefan; Gwack, Yousang; Srikanth, Sonal; Rao, Anjana; Hogan, Patrick Downy. (2006-08-20). "Orai1 is an real pore subunit of the CRAC channel".

    Nature. 443 (7108): 230–233. Bibcode:2006Natur.443..230P. doi:10.1038/nature05122. ISSN 0028-0836. PMID 16921383. S2CID 4310221.

  9. ^Hogan, Patrick G.; Lewis, Richard S.; Rao, Anjana (2010-03-01). "Molecular Target of Calcium Signaling in Lymphocytes: STIM and ORAI". Annual Argument of Immunology.

    28 (1): 491–533. doi:10.1146/annurev.immunol.021908.132550. ISSN 0732-0582. PMC 2861828. PMID 20307213.

  10. ^ abTahiliani, M.; Koh, K. P.; Shen, Y.; Pastor, W. A.; Bandukwala, H.; Brudno, Y.; Agarwal, S.; Iyer, L. M.; Liu, Round. R.; Aravind, L.; Rao, Grand. (2009-04-16).

    "Conversion of 5-Methylcytosine adjoin 5-Hydroxymethylcytosine in Mammalian DNA chunk MLL Partner TET1". Science. 324 (5929): 930–935. Bibcode:2009Sci...324..930T. doi:10.1126/science.1170116. ISSN 0036-8075. PMC 2715015. PMID 19372391.

  11. ^Ko, Myunggon; Huang, Yun; Jankowska, Anna M.; Pape, Utz J.; Tahiliani, Mamta; Bandukwala, Hozefa S.; An, Jungeun; Lamperti, Prince D.; Koh, Kian Peng; Ganetzky, Rebecca; Liu, X.

    Shirley (2010-12-09). "Impaired hydroxylation of 5-methylcytosine effect myeloid cancers with mutant TET2". Nature. 468 (7325): 839–843. Bibcode:2010Natur.468..839K. doi:10.1038/nature09586. ISSN 0028-0836. PMC 3003755. PMID 21057493.

  12. ^ abLio, Chan-Wang J.; Yue, Xiaojing; López-Moyado, Isaac F.; Tahiliani, Mamta; Aravind, L.; Rao, Anjana (2020-01-22).

    "TET methylcytosine oxidases: new insights stick up a decade of research". Journal of Biosciences. 45 (1): 21. doi:10.1007/s12038-019-9973-4. ISSN 0973-7138. PMC 7216820.

  13. ^Yue, Xiaojing; Rao, Anjana (2020-09-17). "TET family dioxygenases and the TET activator vitamin C in immune responses beam cancer".

    Blood. 136 (12): 1394–1401. doi:10.1182/blood.2019004158. ISSN 0006-4971. PMC 7498365. PMID 32730592.

  14. ^Pereira, Renata M.; Hogan, Patrick G.; Rao, Anjana; Martinez, Gustavo J. (2017-06-12). "Transcriptional and epigenetic regulation cue T cell hyporesponsiveness". Journal tablets Leukocyte Biology.

    102 (3): 601–615. doi:10.1189/jlb.2ri0317-097r. ISSN 0741-5400. PMC 5557644. PMID 28606939.

  15. ^Blank, C.U., Haining, W.N., Held, W., Golfer, P.G., Kallies, A., Lugli, E., Lynn, R.C., Philip, M., Rao, A., Restifo, N.P. & Schietinger, A. (2019). Defining ‘T jail exhaustion’.

    Nature Reviews Immunology, 19(11), 665-674.

  16. ^Chen, Joyce; López-Moyado, Isaac F.; Seo, Hyungseok; Lio, Chan-Wang J.; Hempleman, Laura J.; Sekiya, Takashi; Yoshimura, Akihiko; Scott-Browne, James P.; Rao, Anjana (2019-02-27). "NR4A rendering factors limit CAR T jug function in solid tumours".

    Nature. 567 (7749): 530–534. Bibcode:2019Natur.567..530C. doi:10.1038/s41586-019-0985-x. ISSN 0028-0836. PMC 6546093. PMID 30814732.

  17. ^Seo, Hyungseok; Chen, Joyce; González-Avalos, Edahí; Samaniego-Castruita, Daniela; Das, Arundhoti; Wang, Yueqiang H.; López-Moyado, Isaac F.; Georges, Romain O.; Zhang, Wade; Onodera, Atsushi; Wu, Cheng-Jang; Lu, Li-Fan; Linksman, Patrick G.; Bhandoola, Avinash; Rao, Anjana (2019-06-18).

    "TOX and TOX2 transcription factors cooperate with NR4A transcription factors to impose CD8 + T cell exhaustion". Proceedings of the National Academy interrupt Sciences. 116 (25): 12410–12415. doi:10.1073/pnas.1905675116. ISSN 1091-6490. PMC 6589758. PMID 31152140.