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dc.contributor.author Lin, Chih-Wei -
dc.contributor.author Xie, Jia -
dc.contributor.author Zhang, Ding -
dc.contributor.author Han, Kyung Ho -
dc.contributor.author Grande, Geramie -
dc.contributor.author Wu, Nicholas C. -
dc.contributor.author Yang, Zhuo -
dc.contributor.author Yea, Kyungmoo -
dc.contributor.author Lerner, Richard A. -
dc.date.accessioned 2020-02-27T09:12:21Z -
dc.date.available 2020-02-27T09:12:21Z -
dc.date.created 2020-01-29 -
dc.date.issued 2020-01 -
dc.identifier.citation Proceedings of the National Academy of Sciences of the United States of America, v.117, no.1, pp.426 - 431 -
dc.identifier.issn 0027-8424 -
dc.identifier.uri http://hdl.handle.net/20.500.11750/11425 -
dc.description.abstract Herein we present a concept in cancer where an immune response is detrimental rather than helpful. In the cancer setting, the immune system is generally considered to be helpful in curtailing the initiation and progression of tumors. In this work we show that a patient’s immune response to their tumor can, in fact, either enhance or inhibit tumor cell growth. Two closely related autoantibodies to the growth factor receptor TrkB were isolated from cancer patients’ B cells. Although highly similar in sequence, one antibody was an agonist while the other was an antagonist. The agonist antibody was shown to increase breast cancer cell growth both in vitro and in vivo, whereas the antagonist antibody inhibited growth. From a mechanistic point of view, we showed that binding of the agonist antibody to the TrkB receptor was functional in that it initiated downstream signaling identical to its natural growth factor ligand, brain-derived neurotrophic factor (BDNF). Our study shows that individual autoantibodies may play a role in cancer patients. © 2020 National Academy of Sciences. All rights reserved. -
dc.language English -
dc.publisher National Academy of Sciences -
dc.title Immunity against cancer cells may promote their proliferation and metastasis -
dc.type Article -
dc.identifier.doi 10.1073/pnas.1916833117 -
dc.identifier.wosid 000506001200063 -
dc.identifier.scopusid 2-s2.0-85077652273 -
dc.type.local Article(Overseas) -
dc.type.rims ART -
dc.description.journalClass 1 -
dc.citation.publicationname Proceedings of the National Academy of Sciences of the United States of America -
dc.contributor.nonIdAuthor Lin, Chih-Wei -
dc.contributor.nonIdAuthor Xie, Jia -
dc.contributor.nonIdAuthor Zhang, Ding -
dc.contributor.nonIdAuthor Han, Kyung Ho -
dc.contributor.nonIdAuthor Grande, Geramie -
dc.contributor.nonIdAuthor Wu, Nicholas C. -
dc.contributor.nonIdAuthor Yang, Zhuo -
dc.contributor.nonIdAuthor Lerner, Richard A. -
dc.identifier.citationVolume 117 -
dc.identifier.citationNumber 1 -
dc.identifier.citationStartPage 426 -
dc.identifier.citationEndPage 431 -
dc.identifier.citationTitle Proceedings of the National Academy of Sciences of the United States of America -
dc.type.journalArticle Article -
dc.description.isOpenAccess N -
dc.subject.keywordAuthor agonist -
dc.subject.keywordAuthor antibody -
dc.subject.keywordAuthor cancer -
dc.subject.keywordPlus TRKB -
dc.subject.keywordPlus MUTATIONS -
dc.subject.keywordPlus EMT -
dc.subject.keywordPlus AUTOANTIBODIES -
dc.subject.keywordPlus ANTIBODIES -
dc.subject.keywordPlus TRANSITION -
dc.subject.keywordPlus OVARIAN -
dc.contributor.affiliatedAuthor Lin, Chih-Wei -
dc.contributor.affiliatedAuthor Xie, Jia -
dc.contributor.affiliatedAuthor Zhang, Ding -
dc.contributor.affiliatedAuthor Han, Kyung Ho -
dc.contributor.affiliatedAuthor Grande, Geramie -
dc.contributor.affiliatedAuthor Wu, Nicholas C. -
dc.contributor.affiliatedAuthor Yang, Zhuo -
dc.contributor.affiliatedAuthor Yea, Kyungmoo -
dc.contributor.affiliatedAuthor Lerner, Richard A. -
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Department of New Biology Protein Engineering Lab 1. Journal Articles

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