دورية أكاديمية

Appearance of peanut agglutinin in the blood circulation after peanut ingestion promotes endothelial secretion of metastasis-promoting cytokines.

التفاصيل البيبلوغرافية
العنوان: Appearance of peanut agglutinin in the blood circulation after peanut ingestion promotes endothelial secretion of metastasis-promoting cytokines.
المؤلفون: Wang W; The Henry Wellcome Laboratory of Molecular and Cellular Gastroenterology, Institute of Systems, Molecular and Integrative Biology, University of Liverpool, Liverpool L69 3GE, UK., Sindrewicz-Goral P; The Henry Wellcome Laboratory of Molecular and Cellular Gastroenterology, Institute of Systems, Molecular and Integrative Biology, University of Liverpool, Liverpool L69 3GE, UK., Chen C; The Henry Wellcome Laboratory of Molecular and Cellular Gastroenterology, Institute of Systems, Molecular and Integrative Biology, University of Liverpool, Liverpool L69 3GE, UK., Duckworth CA; The Henry Wellcome Laboratory of Molecular and Cellular Gastroenterology, Institute of Systems, Molecular and Integrative Biology, University of Liverpool, Liverpool L69 3GE, UK., Pritchard DM; The Henry Wellcome Laboratory of Molecular and Cellular Gastroenterology, Institute of Systems, Molecular and Integrative Biology, University of Liverpool, Liverpool L69 3GE, UK., Rhodes JM; The Henry Wellcome Laboratory of Molecular and Cellular Gastroenterology, Institute of Systems, Molecular and Integrative Biology, University of Liverpool, Liverpool L69 3GE, UK., Yu LG; The Henry Wellcome Laboratory of Molecular and Cellular Gastroenterology, Institute of Systems, Molecular and Integrative Biology, University of Liverpool, Liverpool L69 3GE, UK.
المصدر: Carcinogenesis [Carcinogenesis] 2021 Aug 19; Vol. 42 (8), pp. 1079-1088.
نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't
اللغة: English
بيانات الدورية: Publisher: Irl Press At Oxford University Press Country of Publication: England NLM ID: 8008055 Publication Model: Print Cited Medium: Internet ISSN: 1460-2180 (Electronic) Linking ISSN: 01433334 NLM ISO Abbreviation: Carcinogenesis Subsets: MEDLINE
أسماء مطبوعة: Publication: Oxford : Irl Press At Oxford University Press
Original Publication: [New York, IRL Press]
مواضيع طبية MeSH: Arachis*, Cytokines/*metabolism , Neoplasm Metastasis/*pathology , Peanut Agglutinin/*blood, Animals ; Cell Adhesion Molecules/metabolism ; Cells, Cultured ; Endothelium, Vascular/drug effects ; Endothelium, Vascular/metabolism ; Female ; Humans ; Inflammation Mediators/metabolism ; Mice ; Mice, Inbred BALB C ; Mucin-1/metabolism ; Peanut Agglutinin/pharmacology ; Signal Transduction
مستخلص: Peanut agglutinin (PNA) is a carbohydrate-binding protein in peanuts that accounts for ~0.15% peanut weight. PNA is highly resistant to cooking and digestion and is rapidly detectable in the blood after peanut consumption. Our previous studies have shown that circulating PNA mimics the actions of endogenous galactoside-binding protein galectin-3 by interaction with tumour cell-associated MUC1 and promotes circulating tumour cell metastatic spreading. The present study shows that circulating PNA interacts with micro- as well as macro-vascular endothelial cells and induces endothelial secretion of cytokines MCP-1 (CCL2) and IL-6 in vitro and in vivo. The increased secretion of these cytokines autocrinely/paracrinely enhances the expression of endothelial cell surface adhesion molecules including integrins, VCAM and selectin, leading to increased tumour cell-endothelial adhesion and endothelial tubule formation. Binding of PNA to endothelial surface MCAM (CD146), via N-linked glycans, and subsequent activation of PI3K-AKT-PREAS40 signalling is here shown responsible for PNA-induced secretion of MCP-1 and IL-6 by vascular endothelium. Thus, in addition to its influence on promoting tumour cell spreading by interaction with tumour cell-associated MUC1, circulating PNA might also influence metastasis by enhancing the secretion of metastasis-promoting MCP-1 and IL-6 from the vascular endothelium.
(© The Author(s) 2021. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com.)
References: J Natl Cancer Inst. 1992 Sep 16;84(18):1410-6. (PMID: 1512792)
J Cell Sci. 2001 Aug;114(Pt 16):2903-10. (PMID: 11686294)
J Immunol. 1996 Feb 15;156(4):1515-24. (PMID: 8568255)
Proc Natl Acad Sci U S A. 1989 Dec;86(24):9891-5. (PMID: 2602381)
Molecules. 2016 Nov 11;21(11):. (PMID: 27845732)
Cell Res. 2015 Mar;25(3):275-87. (PMID: 25656845)
Nature. 2008 Jul 24;454(7203):436-44. (PMID: 18650914)
Exp Mol Pathol. 2016 Jun;100(3):409-15. (PMID: 27079772)
Blood. 2012 Sep 13;120(11):2330-9. (PMID: 22718841)
Glycoconj J. 2007 Nov;24(8):411-20. (PMID: 17457671)
Semin Cancer Biol. 2004 Jun;14(3):149-54. (PMID: 15246049)
Clin Cancer Res. 2013 Apr 1;19(7):1693-704. (PMID: 23401226)
Gastroenterology. 2002 Jun;122(7):1784-92. (PMID: 12055585)
J Biol Chem. 2007 Jan 5;282(1):773-81. (PMID: 17090543)
Br J Cancer. 2016 Jul 26;115(3):371-4. (PMID: 27280637)
Blood. 2000 Jul 1;96(1):34-40. (PMID: 10891427)
Lancet. 1998 Dec 5;352(9143):1831-2. (PMID: 9851393)
Eur J Cancer. 2010 May;46(7):1223-31. (PMID: 20335016)
N Engl J Med. 2013 Nov 21;369(21):2001-11. (PMID: 24256379)
Oncotarget. 2016 May 10;7(19):28697-710. (PMID: 26885690)
Cell Death Differ. 2017 Nov;24(11):1937-1947. (PMID: 28731466)
Clin Cancer Res. 2011 Nov 15;17(22):7035-46. (PMID: 21933892)
Biochem Soc Trans. 2018 Dec 17;46(6):1449-1462. (PMID: 30467123)
Oncogene. 2016 Oct 6;35(40):5317-5327. (PMID: 27041577)
Cell. 2009 Dec 24;139(7):1315-26. (PMID: 20064377)
FEBS Lett. 2003 Apr 10;540(1-3):7-14. (PMID: 12681475)
Cancer Res. 2009 Sep 1;69(17):6799-806. (PMID: 19690136)
J Biol Chem. 2017 May 19;292(20):8381-8389. (PMID: 28364041)
PLoS One. 2013;8(3):e58791. (PMID: 23527025)
Gastroenterology. 1994 Jan;106(1):117-24. (PMID: 8276172)
J Biol Chem. 2014 Mar 14;289(11):7747-62. (PMID: 24415757)
Clin Cancer Res. 2011 Oct 1;17(19):6125-9. (PMID: 21685479)
Carcinogenesis. 2014 Dec;35(12):2815-21. (PMID: 25326505)
Oncogene. 2003 Mar 13;22(10):1517-27. (PMID: 12629515)
Oncotarget. 2017 Apr 20;8(40):69076-69085. (PMID: 28978182)
J Biol Chem. 2008 Jun 6;283(23):15619-27. (PMID: 18372248)
Mol Cancer. 2010 Jun 18;9:154. (PMID: 20565834)
J Cell Biochem. 2020 Apr;121(4):2828-2838. (PMID: 31692069)
Cancer Sci. 2019 Jul;110(7):2090-2099. (PMID: 31111571)
Oncotarget. 2016 Mar 29;7(13):15632-47. (PMID: 26701209)
Oral Oncol. 2017 Jun;69:38-45. (PMID: 28559019)
Int J Cancer. 2003 Feb 20;103(5):642-6. (PMID: 12494472)
J Pathol. 1999 Sep;189(1):4-11. (PMID: 10451481)
Prostate. 2011 Sep 15;71(13):1455-65. (PMID: 21321981)
Cancer Lett. 2013 Apr 28;330(2):150-62. (PMID: 23266426)
Cancer Lett. 2011 Dec 27;313(2):123-8. (PMID: 21974805)
J Cell Biol. 1996 Dec;135(6 Pt 1):1655-68. (PMID: 8978830)
Nat Rev Cancer. 2020 Feb;20(2):74-88. (PMID: 31686003)
Cancer Metastasis Rev. 2006 Dec;25(4):611-9. (PMID: 17160712)
معلومات مُعتمدة: 10A001 American Institute for Cancer Research
المشرفين على المادة: 0 (Cell Adhesion Molecules)
0 (Cytokines)
0 (Inflammation Mediators)
0 (MUC1 protein, human)
0 (Mucin-1)
0 (Peanut Agglutinin)
تواريخ الأحداث: Date Created: 20210705 Date Completed: 20211220 Latest Revision: 20211220
رمز التحديث: 20231215
مُعرف محوري في PubMed: PMC8643467
DOI: 10.1093/carcin/bgab059
PMID: 34223877
قاعدة البيانات: MEDLINE
الوصف
تدمد:1460-2180
DOI:10.1093/carcin/bgab059