The Silkworm Carboxypeptidase Inhibitor Prevents Gastric Cancer Cells' Proliferation through the EGF/EGFR Signaling Pathway.

Junhong Ye, Jifu Li, Ping Zhao
Author Information
  1. Junhong Ye: State Key Laboratory of Silkworm Genome Biology, Biological Science Research Center, Southwest University, Chongqing 400716, China. ORCID
  2. Jifu Li: College of Sericulture, Textile and Biomass Sciences, Southwest University, Chongqing 400716, China.
  3. Ping Zhao: State Key Laboratory of Silkworm Genome Biology, Biological Science Research Center, Southwest University, Chongqing 400716, China.

Abstract

Gastric cancer is a common malignant tumor originating from the gastric mucosa epithelium. Studies have shown that bioactive substances such as antimicrobial peptides and cantharidin contained in a variety of insects can exert anti-cancer functions; when compared with chemotherapy drugs, these bioactive substances have less toxicity and reduced side effects. Here, we report the first Carboxypeptidase inhibitor that is specifically and highly expressed in silk glands, which can significantly prevent the proliferation of Gastric cancer cells by inhibiting the MAPK/ERK pathway initiated by EGF/EGFR through the promotion of expression of the proto-oncogene c-Myc, thereby affecting the expression of related cyclins. Through molecular docking and virtual screening of Silkworm Carboxypeptidase inhibitors and epidermal growth factor receptors, we identified a polypeptide that overlapped with existing small-molecule inhibitors of the receptor. In the present work, we explore the medicinal potential and application of Silkworm Carboxypeptidase inhibitors to promote the development of anti-tumor drugs from insect-derived substances.

Keywords

References

  1. Integr Cancer Ther. 2021 Jan-Dec;20:15347354211045349 [PMID: 34590499]
  2. Eur J Pharmacol. 2003 Feb 14;461(2-3):181-9 [PMID: 12586213]
  3. Front Oncol. 2021 Jun 15;11:639745 [PMID: 34211836]
  4. Helicobacter. 2016 Sep;21 Suppl 1:39-44 [PMID: 27531538]
  5. J Clin Oncol. 2016 Feb 10;34(5):401-3 [PMID: 26700116]
  6. Oncol Lett. 2014 Jan;7(1):255-259 [PMID: 24348859]
  7. Annu Rev Pathol. 2011;6:49-69 [PMID: 20887192]
  8. Int J Mol Sci. 2020 Jun 04;21(11): [PMID: 32512697]
  9. J Pharm Sci. 2000 Feb;89(2):145-54 [PMID: 10688744]
  10. J Gastrointest Oncol. 2015 Feb;6(1):60-74 [PMID: 25642339]
  11. Curr Opin Gastroenterol. 2018 Nov;34(6):465-468 [PMID: 30303856]
  12. Oncotarget. 2017 Jul 14;8(34):57187-57200 [PMID: 28915664]
  13. Biochim Biophys Acta. 2007 Aug;1773(8):1263-84 [PMID: 17126425]
  14. Proc Natl Acad Sci U S A. 2009 Feb 10;106(6):1743-7 [PMID: 19179285]
  15. Arch Biochem Biophys. 2022 Jan 15;715:109095 [PMID: 34826396]
  16. Crit Rev Oncog. 2007 Nov;13(2):93-158 [PMID: 18197790]
  17. Int J Oncol. 2021 Nov;59(5): [PMID: 34558640]
  18. Cancer Metastasis Rev. 2020 Dec;39(4):1179-1203 [PMID: 32894370]
  19. Food Chem. 2021 Jul 30;351:129338 [PMID: 33647700]
  20. Plant Biotechnol J. 2007 Jul;5(4):537-53 [PMID: 17547659]
  21. Eur J Biochem. 2001 Apr;268(7):2064-73 [PMID: 11277929]
  22. J Biol Chem. 2015 Oct 9;290(41):25103-17 [PMID: 26306031]
  23. World J Gastroenterol. 2015 Mar 7;21(9):2711-8 [PMID: 25759540]
  24. Cells. 2021 Jan 21;10(2): [PMID: 33494237]
  25. J Biol Chem. 1998 May 15;273(20):12370-7 [PMID: 9575190]
  26. Aging (Albany NY). 2020 Feb 24;12(4):3574-3593 [PMID: 32091407]
  27. Biochemistry. 1976 Jun 15;15(12):2573-8 [PMID: 938626]
  28. Future Sci OA. 2020 Jan 24;6(3):FSO451 [PMID: 32140250]
  29. Clin Transl Oncol. 2008 Jan;10(1):6-13 [PMID: 18208787]
  30. Cell Cycle. 2011 Jan 1;10(1):57-67 [PMID: 21200143]
  31. Endocr Relat Cancer. 2005 Jul;12 Suppl 1:S47-59 [PMID: 16113099]
  32. PLoS One. 2012;7(2):e31168 [PMID: 22348050]
  33. Cancer. 1995 Mar 15;75(6 Suppl):1418-25 [PMID: 7889468]
  34. Int J Mol Sci. 2020 Mar 05;21(5): [PMID: 32150871]
  35. Chemosphere. 2022 Nov;306:135578 [PMID: 35798154]
  36. Cell. 2012 Mar 30;149(1):22-35 [PMID: 22464321]
  37. Sci Rep. 2016 Apr 22;6:21158 [PMID: 27102218]
  38. Mol Oncol. 2018 Jan;12(1):3-20 [PMID: 29124875]
  39. Int J Mol Sci. 2016 Jul 28;17(8): [PMID: 27483237]
  40. Bioorg Chem. 2020 Jun;99:103811 [PMID: 32278207]
  41. J Med Chem. 2005 Aug 11;48(16):5321-8 [PMID: 16078849]
  42. Infect Genet Evol. 2020 Nov;85:104502 [PMID: 32798769]
  43. BMC Cancer. 2011 Apr 06;11:121 [PMID: 21466706]
  44. Expert Opin Pharmacother. 2014 Apr;15(5):717-28 [PMID: 24588695]
  45. Lancet. 2020 Aug 29;396(10251):635-648 [PMID: 32861308]
  46. Curr Top Med Chem. 2020;20(10):815-834 [PMID: 32124699]
  47. Indian J Biochem Biophys. 2003 Apr;40(2):139-42 [PMID: 22900303]
  48. Front Pharmacol. 2021 Jul 20;12:690875 [PMID: 34354587]
  49. ACS Med Chem Lett. 2021 Nov 17;12(12):1948-1954 [PMID: 34917259]
  50. Eur J Med Chem. 2019 Dec 1;183:111682 [PMID: 31563805]
  51. CA Cancer J Clin. 2018 Nov;68(6):394-424 [PMID: 30207593]
  52. Insect Biochem Mol Biol. 2012 Oct;42(10):766-75 [PMID: 22841512]
  53. Eur J Biochem. 1999 Jan;259(1-2):120-6 [PMID: 9914483]
  54. CA Cancer J Clin. 2021 May;71(3):264-279 [PMID: 33592120]
  55. Semin Cancer Biol. 2020 Apr;61:167-179 [PMID: 31562956]
  56. Comp Biochem Physiol B Biochem Mol Biol. 2005 Jul;141(3):314-22 [PMID: 15936966]
  57. Ital J Surg Sci. 1987;17(2):141-6 [PMID: 3038783]
  58. J Biol Chem. 2005 Feb 4;280(5):3441-8 [PMID: 15561703]
  59. J Cell Mol Med. 2020 Jul;24(13):7151-7162 [PMID: 32530106]

Grants

  1. 32172798/National Natural Science Foundation of China
  2. 32030103/National Natural Science Foundation of China
  3. cstc2020jcyjcxtt-X0001/Chongqing Natural Science Foundation for Innovation Group Science Foundation

MeSH Term

Animals
Humans
Bombyx
Epidermal Growth Factor
Stomach Neoplasms
Molecular Docking Simulation
Signal Transduction
ErbB Receptors
Antineoplastic Agents
Cell Proliferation
Carboxypeptidases

Chemicals

Epidermal Growth Factor
ErbB Receptors
Antineoplastic Agents
Carboxypeptidases
EGFR protein, human

Word Cloud

Created with Highcharts 10.0.0carboxypeptidasecancergastricsubstancessilkworminhibitorsGastricbioactivecandrugsinhibitorEGF/EGFRexpressionanti-tumorcommonmalignanttumororiginatingmucosaepitheliumStudiesshownantimicrobialpeptidescantharidincontainedvarietyinsectsexertanti-cancerfunctionscomparedchemotherapylesstoxicityreducedsideeffectsreportfirstspecificallyhighlyexpressedsilkglandssignificantlypreventproliferationcellsinhibitingMAPK/ERKpathwayinitiatedpromotionproto-oncogenec-Myctherebyaffectingrelatedcyclinsmoleculardockingvirtualscreeningepidermalgrowthfactorreceptorsidentifiedpolypeptideoverlappedexistingsmall-moleculereceptorpresentworkexploremedicinalpotentialapplicationpromotedevelopmentinsect-derivedSilkwormCarboxypeptidaseInhibitorPreventsCancerCells'ProliferationSignalingPathwayactivity

Similar Articles

Cited By