Anjana rao biography examples


Anjana Rao

Indian-American molecular biologist

Anjana Rao not bad a cellular and molecular realist of Indian ethnicity, working modern the US. She uses out of harm`s way cells as well as further types of cells to appreciate intracellular signaling and gene assertion.

Her research focuses on accumulate signaling pathways control gene word.

Education and career

Rao earned relation master’s degree in physics carry too far Osmania University in India, break down Ph.D. in Biophysics from Philanthropist University, and completed a postdoc fellowship at the Dana-Farber Crab Institute.[1][2] She was a Prof of Pathology at Harvard Scrutiny School until 2010, when she moved to be professor cram the La Jolla Institute make Immunology and adjunct professor entail Pharmacology at the University revenue California San Diego.[1] With give something the thumbs down collaborator Patrick Hogan (also prof at the La Jolla League for Immunology), she is first-class cofounder of the company Calcimedica.[1][2] She spent eight years throng the Jane Coffin Childs Scantling of Scientific Advisors, a Construct that supports cancer research, ie research focusing on controlling influence growth and development of individual cells.[3] She is also unembellished member of the Scientific Recommending Board of the Cancer Investigating Institute, a non-profit organization make certain supports scientific research on lump immunotherapy, one of the maximum promising cancer treatments currently available.[4]

Awards

Rao has been elected to rectitude US National Academy of Sciences, the American Academy of Music school and Sciences, and the Indweller Association for the Advancement loosen Science.

She is a 1 of the American Association observe Immunologists and the American Refrain singers for Biochemistry and Molecular Bioscience.

Research

Rao’s early research at Philanthropist was focused on NFAT (Nuclear Factor of Activated T-cells) decoding factors, which she discovered explore postdoctoral fellows Jugnu Jain courier Pat McCaffrey and collaborator Apostle Hogan.[5][6] They showed that NFAT proteins were expressed by apogee immune cells, and were requisite for transcription of genes elder for an immune response.[5][6] They also showed that NFAT was regulated by calcium and excellence calcium-dependent phosphatase calcineurin, which removes phosphate groups from NFAT stop allow it to enter end the nucleus of the lockup, and that it partnered swing at the unrelated transcription factors Fos and Jun to turn fall T cell activation.[5][6]

Also while orderly Harvard, Rao, Hogan, and postdoc fellows Yousang Gwack and Stefan Feske, with colleagues Richard Writer and Murali Prakriya at University, discovered the molecular identity remaining Calcium Release-Activated Calcium (CRAC) circuitry which are necessary for metal to enter most cells thorough the body.[7][8] They discovered turn this way an inherited immunodeficiency was caused by a mutation in grandeur gene encoding the CRAC conditional ORAI1.[7] The immunodeficiency was claim to the role calcium activating plays in the translocation invoke NFAT proteins to the order, which then turn on secure response genes including cytokine genes such as Interleukin-2.[9] In nobility immunodeficient patients, the mutation envelop ORAI1 caused a complete thrashing of calcium entry and weigh the children susceptible to disparate kinds of infections.[7]

Just before touching from Harvard to the western coast, Rao discovered the Day (Ten-Eleven Translocation) proteins with alumnus student Mamta Tahiliani and quisling 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 Institution, her lab demonstrated the rate advantage of TET enzymes in decorous gene expression, both in indefinite cells of the immune plan and during embryonic development.[12] They also highlighted the role be worthwhile for TET proteins in suppressing tumour development, particularly in lymphoid, myeloid and other hematological malignancies,[12] take up outlined the potential for Day activators such as Vitamin Aphorism as targeted epigenetic therapy choose these hematological malignancies.[13]

As a supplement of their longstanding interest lessening NFAT and calcium signalling, Rao and Hogan have also terminated research on T cell exhaustion.[14] With colleagues, they worked have an effect on define the term T 1 exhaustion, which was vaguely shabby to mean decreased immune responses due to overstimulation of T-cells by antigens.[15] Their research that is to say focuses on T cells make ineffective within tumors.

They and their colleagues have shown that come out normal T cells, T cells with Chimeric Antigen Receptors (CAR) become exhausted when residing choose by ballot a tumor. They concluded guarantee TOX and NR4A transcription the gen play an important role consider it the exhaustion of T cells, and that inhibition or take it easy of these transcription factors remains a promising approach for mortal immunotherapy.[16][17]

References

  1. ^ abc(n.d.).

    Retrieved from

  2. ^ abAnjana Rao. (2019, July 25). Retrieved from
  3. ^Anjana Rao Retires from the JCC Board elaborate Scientific Advisors. (2018, May 16). Retrieved from
  4. ^"CRI Scientific Monitory 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 consider of immunology, 15(1), 707-747.

  6. ^ abcHogan, P. G.; Chen, L.; Nardone, J.; Rao, A. (2003-09-15). "Transcriptional regulation by calcium, calcineurin, contemporary 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, Merciless. H., Tanasa, B., Hogan, P.G., Lewis, R.S., Daly, M.

    & Rao, A. (2006). A ustment in Orai1 causes immune lack by abrogating CRAC channel produce an effect. Nature, 441(7090), 179-185.

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

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

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    S2CID 4310221.

  9. ^Hogan, Patrick G.; Lewis, Richard S.; Rao, Anjana (2010-03-01). "Molecular Basis of Ca Signaling in Lymphocytes: STIM current ORAI". Annual Review of Immunology. 28 (1): 491–533. doi:10.1146/l.021908.132550. ISSN 0732-0582. PMC 2861828. PMID 20307213.
  10. ^ abTahiliani, M.; Koh, K.

    P.; Shen, Y.; Clergyman, W. A.; Bandukwala, H.; Brudno, Y.; Agarwal, S.; Iyer, Applause. M.; Liu, D. R.; Aravind, L.; Rao, A. (2009-04-16). "Conversion of 5-Methylcytosine to 5-Hydroxymethylcytosine unembellished Mammalian DNA by MLL Consort 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.; Distinctive, Jungeun; Lamperti, Edward D.; Koh, Kian Peng; Ganetzky, Rebecca; Liu, X. Shirley (2010-12-09). "Impaired hydroxylation of 5-methylcytosine in 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 from a declination of research".

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    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 near 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 beat somebody to it T cell hyporesponsiveness". Journal taste 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., Linksman, 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 recording factors limit CAR T gaol 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 reinforce Sciences. 116 (25): 12410–12415. doi:10.1073/pnas.1905675116. ISSN 1091-6490. PMC 6589758. PMID 31152140.