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John Vane

From Wikipedia, the free encyclopedia
British scientist
For the Australian bushranger, seeJohn Vane (bushranger). For the British peer, seeJohn Vane, 11th Baron Barnard.

Sir John Vane
Born
John Robert Vane

(1927-03-29)29 March 1927
Died19 November 2004(2004-11-19) (aged 77)
Kent, England
CitizenshipUnited Kingdom
Alma mater
Known forResearch onprostaglandins
Spouse
Elizabeth Daphne Page
(m. 1948)
Awards
Scientific career
FieldsPharmacology
Institutions
ThesisBlood flow and its relation to secretion in the stomach and smaller intestine (1952)
Doctoral advisorGeoffrey S. Dawes

Sir John Robert VaneFRS (29 March 1927 – 19 November 2004)[1] was aBritishpharmacologist who was instrumental in the understanding of howaspirin produces pain-relief and anti-inflammatory effects and his work led to new treatments for heart and blood vessel disease and introduction ofACE inhibitors. He was awarded theNobel Prize in Physiology or Medicine in 1982 along withSune Bergström andBengt Samuelsson for "their discoveries concerningprostaglandins and related biologically active substances".[2]

Education and early life

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Born inTardebigge,Worcestershire, John Vane was one of three children and grew up in suburban Birmingham. His father, Maurice Vane, was the son ofJewish Russian immigrants[3] and his mother, Frances Vane, came from aWorcestershire farming family.[2] He attended a local state school from age 5, before moving on toKing Edward's School inEdgbaston,Birmingham. An early interest in chemistry was to prove the inspiration for studyingthe subject at theUniversity of Birmingham in 1944.

During his undergraduate studies, Vane became disenchanted with chemistry but still enjoyed experimentation. WhenMaurice Stacey, the Professor of Chemistry at Birmingham, was asked byHarold Burn to recommend a student to go to Oxford and study pharmacology, Vane jumped at the chance and moved to Burn's department in 1946. Under Burn's guidance, Vane found motivation and enthusiasm for pharmacology, writing:"[the] laboratory gradually became the most active and important centre for pharmacological research in the U.K. and the main school for training of young pharmacologists."[2] Vane completed aBachelor of Science degree inpharmacology and briefly went to work at theUniversity of Sheffield,[citation needed] before coming back to Oxford to complete hisDoctor of Philosophy degree in 1953[4] supervised byGeoffrey Dawes.[5]

Career and research

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After completing his DPhil, Vane worked as an assistant professor the Department of Pharmacology atYale University before moving back to the United Kingdom to take up a post as a senior lecturer in the Institute of Basic Medical Sciences at theUniversity of London in 1955.[6][7]

University of London

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John Vane andSalvador Moncada in the 1960s

Vane held a post at theUniversity of London for 18 years, progressing from senior lecturer to Professor of Experimental Pharmacology in 1966 (at the Royal College of Surgeons). During that time he developed certainbioassay techniques and focussed his research on bothangiotensin-converting enzyme and the actions of aspirin, eventually leading to the publication with Priscilla Piper of the relationship between aspirin and the prostaglandins that earned him theNobel Prize in Physiology or Medicine in 1982.[8][9][10][11]

Wellcome Foundation

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In 1973, Vane left his academic post at the Royal College of Surgeons and took up the position as Director of Research at theWellcome Foundation, taking a number of his colleagues with him who went on to form the Prostaglandin Research department. Under the leadership ofSalvador Moncada, this group continued important research that eventually led to the discovery ofprostacyclin.[6]

Return to academia

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In 1985, Vane returned to academic life and founded[12] theWilliam Harvey Research Institute at the Medical College ofSt Bartholomew's Hospital (nowBarts and The London School of Medicine and Dentistry.[13] At the William Harvey Research Institute, Vane's work focused on selective inhibitors ofCOX-2, and the interplay betweennitric oxide andendothelin in the regulation ofvascular function.[6]

Awards and honours

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Vane was elected aFellow of the Royal Society (FRS) in 1974.[1] He was also awarded honorary doctorate degrees fromJagiellonian University Medical College (formerly Copernicus Academy of Medicine) in 1977,Paris Descartes University in 1978,Mount Sinai School of Medicine in 1980, theUniversity of Aberdeen in 1983 andFu Jen Catholic University in 2011.[2][14] He was awarded theLasker Award in 1977 for the discovery of prostacyclin and was knighted in 1984 for his contributions to science. In 2000, Vane received the Golden Plate Award of theAmerican Academy of Achievement.[15]

Personal life

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John Vane married, in 1948, (Elizabeth) Daphne Page and had 2 daughters. He died on 19 November 2004 inPrincess Royal University Hospital,Kent, from long-term complications arising from leg and hip fractures he sustained in May of that year.[16] Lady Vane died in 2021.[17]

See also

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References

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  1. ^abcMoncada, S. (2006)."Sir John Robert Vane. 29 March 1927 -- 19 November 2004: Elected FRS 1974".Biographical Memoirs of Fellows of the Royal Society.52:401–411.doi:10.1098/rsbm.2006.0027.PMID 18551797.S2CID 38582901.
  2. ^abcdJohn R. Vane on Nobelprize.orgEdit this at Wikidata, accessed 12 October 2020
  3. ^According to an interview published in Candid Science II, by István Hargittai (Imperial College Press, London, 2002, p. 562).
  4. ^Vane, John Robert (1952).Blood flow and its relation to secretion in the stomach and smaller intestine (DPhil thesis). University of Oxford.
  5. ^Liggins, G. (1998)."Geoffrey Sharman Dawes, C. B. E. 21 January 1918-6 May 1996".Biographical Memoirs of Fellows of the Royal Society.44:111–125.doi:10.1098/rsbm.1998.0008.PMID 11623979.
  6. ^abc"Sir John R. Vane FRS, Nobel Laureate (1927–2004)"Archived 27 January 2013 at theWayback Machine. William Harvey Research Foundation.
  7. ^John Vane publications indexed byMicrosoft Academic
  8. ^Moncada; Ferreira, SH; Vane, JR (1975). "Inhibition of prostaglandin biosynthesis as the mechanism of analgesia of aspirin-like drugs in the dog knee joint".European Journal of Pharmacology.31 (2):250–60.doi:10.1016/0014-2999(75)90047-3.PMID 1149792.
  9. ^Ferreira; Moncada, S; Vane, JR (1973)."Further experiments to establish that the analgesic action of aspirin-like drugs depends on the inhibition of prostaglandin biosynthesis".British Journal of Pharmacology.47 (3):629P–630P.doi:10.1111/j.1476-5381.1973.tb08193.x.PMC 1776306.PMID 4199867.
  10. ^Ferreira; Moncada, S; Vane, JR (1971). "Indomethacin and aspirin abolish prostaglandin release from the spleen".Nature New Biology.231 (25):237–9.doi:10.1038/newbio231237a0.PMID 5284362.
  11. ^Vane (1971). "Inhibition of prostaglandin synthesis as a mechanism of action for aspirin-like drugs".Nature New Biology.231 (25):232–5.doi:10.1038/newbio231232a0.PMID 5284360.
  12. ^"William Harvey Research Institute".Queen Mary, University of London, UK. Retrieved7 January 2012.
  13. ^"Queen Mary, University of London Notable Alumni and Staff". Archived fromthe original on 12 December 2007. Retrieved23 September 2007.
  14. ^輔仁大學 校史室 >>輔仁歷史軌跡
  15. ^"Golden Plate Awardees of the American Academy of Achievement".www.achievement.org.American Academy of Achievement.
  16. ^Obituary:Sir John Vane. guardian.co.uk. 25 November 2004.
  17. ^VANE Lady, (Elizabeth) Daphne (née Page)

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