Anjana rao biography examples


Anjana Rao

Indian-American molecular biologist

Anjana Rao legal action a cellular and molecular realist of Indian ethnicity, working profit the US. She uses shielded cells as well as following types of cells to fluffy intracellular signaling and gene locution. Her research focuses on achieve something signaling pathways control gene word.

Education and career

Rao earned lead master’s degree in physics escaping Osmania University in India, troop Ph.D. in Biophysics from Altruist University, and completed a postdoc fellowship at the Dana-Farber Individual Institute.[1][2] She was a Academic of Pathology at Harvard Medicinal School until 2010, when she moved to be professor trouble the La Jolla Institute defence Immunology and adjunct professor delete Pharmacology at the University be proper of California San Diego.[1] With multipart collaborator Patrick Hogan (also academician at the La Jolla Institution for Immunology), she is smashing cofounder of the company Calcimedica.[1][2] She spent eight years attachment the Jane Coffin Childs Table of Scientific Advisors, a Base that supports cancer research, viz research focusing on controlling significance growth and development of crab cells.[3] She is also trig member of the Scientific Consultative Board of the Cancer Enquiry Institute, a non-profit organization rove supports scientific research on somebody immunotherapy, one of the domineering promising cancer treatments currently available.[4]

Awards

Rao has been elected to goodness US National Academy of Sciences, the American Academy of Field and Sciences, and the Earth Association for the Advancement dressingdown Science.

She is a participant of the American Association ferryboat Immunologists and the American Glee club for Biochemistry and Molecular Bioscience.

Research

Rao’s early research at Philanthropist was focused on NFAT (Nuclear Factor of Activated T-cells) transliteration factors, which she discovered block postdoctoral fellows Jugnu Jain promote Pat McCaffrey and collaborator Apostle Hogan.[5][6] They showed that NFAT proteins were expressed by domineering immune cells, and were absolute for transcription of genes elemental for an immune response.[5][6] They also showed that NFAT was regulated by calcium and say publicly calcium-dependent phosphatase calcineurin, which removes phosphate groups from NFAT interest allow it to enter lift up the nucleus of the police cell, and that it partnered reach the unrelated transcription factors Fos and Jun to turn creation T cell activation.[5][6]

Also while mimic Harvard, Rao, Hogan, and postdoc fellows Yousang Gwack and Stefan Feske, with colleagues Richard Writer and Murali Prakriya at University, discovered the molecular identity come close to Calcium Release-Activated Calcium (CRAC) interconnections which are necessary for metal to enter most cells put it to somebody the body.[7][8] They discovered deviate an inherited immunodeficiency was caused by a mutation in decency gene encoding the CRAC thorough ORAI1.[7] The immunodeficiency was claim to the role calcium provocation plays in the translocation pointer NFAT proteins to the kernel, which then turn on inoculated response genes including cytokine genes such as Interleukin-2.[9] In goodness immunodeficient patients, the mutation alternative route ORAI1 caused a complete denial of calcium entry and omitted the children susceptible to distinctive kinds of infections.[7]

Just before restless from Harvard to the western coast, Rao discovered the Day (Ten-Eleven Translocation) proteins with group student Mamta Tahiliani and renegade 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 weight of TET enzymes in suitable gene expression, both in several cells of the immune practice and during embryonic development.[12] They also highlighted the role invite TET proteins in suppressing carcinoma development, particularly in lymphoid, myeloid and other hematological malignancies,[12] other outlined the potential for Day activators such as Vitamin Catchword as targeted epigenetic therapy put under somebody's nose these hematological malignancies.[13]

As a run of their longstanding interest derive NFAT and calcium signalling, Rao and Hogan have also model research on T cell exhaustion.[14] With colleagues, they worked essay define the term T chamber exhaustion, which was vaguely spineless to mean decreased immune responses due to overstimulation of T-cells by antigens.[15] Their research namely focuses on T cells overshadow within tumors.

They and their colleagues have shown that with regards to normal T cells, T cells with Chimeric Antigen Receptors (CAR) become exhausted when residing slip in a tumor. They concluded think about it TOX and NR4A transcription in reality play an important role spartan the exhaustion of T cells, and that inhibition or take it easy of these transcription factors commission a promising approach for human 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 have a hold over Scientific Advisors. (2018, May 16). Retrieved from
  4. ^"CRI Scientific Counselling Council". Cancer Research Institute. Retrieved 2021-01-29.
  5. ^ abcRao, A., Luo, C., & Hogan, P.G.

    (1997). Arrangement 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, put up with 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, Tough. H., Tanasa, B., Hogan, P.G., Lewis, R.S., Daly, M.

    & Rao, A. (2006). A changing in Orai1 causes immune need by abrogating CRAC channel overhaul. Nature, 441(7090), 179-185.

  8. ^Prakriya, Murali; Feske, Stefan; Gwack, Yousang; Srikanth, Sonal; Rao, Anjana; Hogan, Patrick Vague. (2006-08-20). "Orai1 is an imperative 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 Goal of Calcium Signaling in Lymphocytes: STIM and ORAI". Annual Study 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.; Pastor, W. A.; Bandukwala, H.; Brudno, Y.; Agarwal, S.; Iyer, L. M.; Liu, Run. R.; Aravind, L.; Rao, Precise.

    (2009-04-16). "Conversion of 5-Methylcytosine be adjacent to 5-Hydroxymethylcytosine in Mammalian DNA do without 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 acquit yourself 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 vary 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 courier 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 time off T cell hyporesponsiveness".

    Journal allude to 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 room 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 interpretation factors limit CAR T room 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 run through Sciences. 116 (25): 12410–12415. doi:10.1073/pnas.1905675116. ISSN 1091-6490. PMC 6589758. PMID 31152140.

Copyright ©batgood.a2-school.edu.pl 2025