Preview

Advances in Molecular Oncology

Advanced search

Exosomal proteases in colorectal cancer

https://doi.org/10.17650/2313-805X-2018-5-4-117-126

Abstract

The objective is to evaluate the level of ADAM10 and ADAM17 (a disintegrin and metalloproteinase) proteases, as well as 20S-proteasomes in blood plasma exosomes of patients with colorectal cancer.

Materials and methods. The study included 60 patients with colorectal cancer (T2–4N0–2M0–1) and 10 control patients. The material for the study was EDTA blood plasma. Exosomes of blood plasma were isolated by ultrafiltration with ultracentrifugation. The level of tetraspanin-associated (ADAM10 and ADAM17) and tetraspanin-non-associated (20S-proteasome) proteases was evaluated by flow cytometry and Western blotting.

Results. A twice negative subpopulation (ADAM10–/ADAM17–) predominated in blood plasma exosomes of colorectal cancer patients and control patients. The level of ADAM10+/ADAM17– exosomes was significantly higher in the exosomes of the plasma of control patients. There were no significant differences between the ADAM10/ADAM17 subpopulations and the 20S-proteasome level, depending on sex, age and tumor grade. A decrease in the ADAM10+/ADAM17– subpopulation was found in patients with metastatic colorectal cancer with hematogenous metastases compared with patients with T2–4N1–2M0 and 20S-proteasome compared to T2–4N0M0. A decrease in ADAM10–/ ADAM17+ exosomes and 20S-proteasomes level was found in exosomes of patients with colorectal cancer with a metabolic syndrome  in comparison with patients without metabolic disorders.

About the Authors

E. A. Zambalova
Cancer Research Institute, Тomsk National Research Medical Center of Russian Academy of Sciences
Russian Federation

5 Kooperativnyy Pereulok, Tomsk 634009



M. R. Patysheva
Cancer Research Institute, Тomsk National Research Medical Center of Russian Academy of Sciences
Russian Federation

5 Kooperativnyy Pereulok, Tomsk 634009



A. A. Dimcha
Cancer Research Institute, Тomsk National Research Medical Center of Russian Academy of Sciences
Russian Federation

5 Kooperativnyy Pereulok, Tomsk 634009



S. N. Tamkovich
Institute of Chemical Biology and Fundamental Medicine, Siberian Branch of Russian Academy of Sciences; Novosibirsk National State Research University
Russian Federation

8 Аkad. Lavrent’eva Rpospekt, Novosibirsk 630090; 2 Pirogova St., Novosibirsk 630090



A. E. Grigor’eva
Institute of Chemical Biology and Fundamental Medicine, Siberian Branch of Russian Academy of Sciences
Russian Federation

8 Аkad. Lavrent’eva Rpospekt, Novosibirsk 630090



E. S. Kolegova
Cancer Research Institute, Тomsk National Research Medical Center of Russian Academy of Sciences
Russian Federation

5 Kooperativnyy Pereulok, Tomsk 634009



I. V. Kondakova
Cancer Research Institute, Тomsk National Research Medical Center of Russian Academy of Sciences
Russian Federation

5 Kooperativnyy Pereulok, Tomsk 634009



S. G. Afanas’ev
Cancer Research Institute, Тomsk National Research Medical Center of Russian Academy of Sciences
Russian Federation

5 Kooperativnyy Pereulok, Tomsk 634009



N. V. Yunusova
Cancer Research Institute, Тomsk National Research Medical Center of Russian Academy of Sciences; Siberian State Medical University
Russian Federation

5 Kooperativnyy Pereulok, Tomsk 634009; 2 Moskovskiy Tract, Tomsk 634050



References

1. Loree J., Kopetz S. Recent developments in the treatment of metastatic colorectal cancer. Ther Adv Med Oncol 2017;9(8):551 —64. DOI: 10.1177/1758834017714997. PMID: 28794806.

2. Li W., Li C., Zhou T. et al. Role of exo-somal proteins in cancer diagnosis. Mol Cancer 2017;16(1):145. DOI: 10.1186/s12943-017-0706-8. PMID: 28851367.

3. Yunusova N.V., Tamkovich S.N., Stakhe-eva M.N. et al. The characterization of exosome from blood plasma of patients with colorectal cancer. AIP Conference Proceedings 2016;1760, № 020070.

4. Yunusova N.V., Tugutova E.A., Tamkovich S.N. et al. The role of exosomal tetraspanins and proteases in tumor progression. Biomeditsins-kaya khimiya = Biomedical Chemistry 2018;64(2):123—33. DOI: 10.18097/PBMC20186402123. (In Russ.).

5. Mathivanan S., Ji H., Simpson R.J. Exo-somes: extracellular organelles important in intercellular communication. J Proteomics 2010;73(10):1907—20. DOI: 10.1016/j.jprot.2010.06.006. PMID: 20601276.

6. Matthews A.L., Noy PJ., Reyat J.S. et al. Regulation of A disintegrin and metalloproteinase (ADAM) family sheddases ADAM10 and ADAM17: The emerging role of tetraspanins and rhomboids. Platelets 2017;28(4):333-41. DOI: 10.1080/09537104.2016.1184751. PMID: 27256961.

7. Lee S.B., Schramme A., Doberstein K. et al. ADAM10 is upregulated in melanoma metastasis compared with primary melanoma. J Invest Dermatol 2010;130(3):763—73. DOI: 10.1038/jid.2009.335. PMID: 19865098.

8. Stoeck A., Keller S., Riedle S. et al. A role for exosomes in the constitutive and stimulus-induced ectodomain cleavage of L1 and CD44. Biochem J 2006;393(3): 609-18. DOI: 10.1042/BJ20051013. PMID: 16229685.

9. Yunusova N.V., Spi-rina L.V., Kondakova I.V et al. Relationship between the expression levels of PAPP-A metalloprotease and growth and transcriptional factors in endometrial cancer. Izvestiya RAN. Seriya biologicheskaya = Biology Bulletin 2013;3:284. (In Russ.) DOI:10.7868/S0002332913030119.

10. Kondakova I.V., Yunusova N.V., Spirina L.V. et al. Association between intracellular proteinase activities and the content of locomotor proteins in tissues of primary tumors and metastases of ovarian cancer. Bioorg Chem 2014;40(6):681-7. PMID: 25895370.

11. Lai R.C., Tan S.S., Teh B.J. et al. Proteolytic potential of the MSC exosome pro-teome: implications for an exosome-mediated delivery of therapeutic proteasome. E N C E S J Proteomics 2012;12:971907. DOI: 10.1155/2012/971907. PMID: 22852084.

12. Sharova N., Zakharova L. Multiple forms of proteasomes and their role in tumor fate. Recent Patients On Endocrine, Metabolic & Immune Drug Discovery 2005;2(3):152—61.

13. Tamkovich S.N., Yunusova N.V., Stakheeva M.N. et al. Isolation and characterization of exosomes from blood plasma of breast cancer and colorectal cancer patients. Biomeditsins-kaya khimiya = Biomedical Chemistry 2017;63(2):165—9. (In Russ.) DOI: 10.18097/PBMC20176302165.

14. Grigorieva A.E., Dyrkheeva N.S., Bryzgunova O.E. et al. Contamination of exosome preparations isolated from biological fluids Biomedit-sinskaya khimiya = Biomedical Chemistry 2017;63(1):91—6. (In Russ.).

15. Tian Y., Ma L., Gong M. et al. Protein profiling and sizing of extracellular vesicles from colorectal cancer patients via flow cytometry. ACS Nano 2018;12(1):671—80. DOI: 10.1021/acsnano.7b07782. PMID: 29300458.

16. Silva J., Garcia V., Rodriguez M. et al. Analysis of exosome release and its prognostic value in human colorectal cancer. Genes Chromosomes Cancer 2012;51(4):409—18. PMID: 22420032.

17. Yoshioka Y., Kosaka N., Konishi Y. et al. Ultra-sensitive liquid biopsy of circulating extracellular vesicles using ExoScreen. Nat Commun 201;5:3591. DOI: 10.1038/ncomms4591. PMID: 24710016.

18. Mathews J.A., Gibb D.R., Chen B.H. et al. CD23 Sheddase A disintegrin and metalloproteinase 10 (ADAM10) is also required for CD23 sorting into B cell-derived exosomes. J Biol Chem 2010;285(48):37531 —41. DOI: 10.1074/jbc.M110.141556. PMID: 20876574.

19. Arduise C., Abache T., Li L. et al. Tet-raspanins regulate ADAM10-mediated cleavage of TNF-alpha and epidermal growth factor. J Immunol 2008;181(10):7002—13. PMID: 18981120.

20. Lopez-Verrilli M.A., Picou F., Court F.A. Schwann cell-derived exosomes enhance axonal regeneration in the peripheral nervous system. Glia 2013;61(11):1795-806. DOI: 10.1002/glia.22558. PMID: 24038411.

21. Groth E., Pruessmeyer J., Babendreyer A. et al. Stimulated release and functional activity of surface expressed metalloproteinase ADAM17 in exosomes. Biochim Bio-phys Acta 2016;1863(11):2795-808. DOI: 10.1016/j.bbamcr.2016.09.002. PMID: 27599715.

22. Zhu Y., Chen X., Pan Q.J. et al. A comprehensive proteomics analysis reveals a secretory path- and status-dependent signature of exosomes released from tumor-associated macrophages. Proteome Res 2015;14(10):4319—31. DOI: 10.1021/acs.jproteome.5b00770.

23. Kondakova I.V., Spirina L.V., Koval V.D. et al. Chymotrypsin-like activity and subunit composition of proteasomes in human cancers. Molekulyarnaya biologiya = Molecular Biology 2014;48(3):384-9. (In Russ.) DOI: 10.7868/S0026898414030112.

24. Yunusova N.V., Kondakova I.V., Kolo-miets L.A. et al. Molecular targets for the therapy of cancer associated with metabolic syndrome (transcription and growth factors). Asia Pac J Clin Oncol 2017;14(3):134—40. DOI: 10.1111/ajco.12780. PMID: 29115033.

25. Yunusova N.V., Kondakova I.V., Kolomiets L.A. et al. Serum adipokines and their receptors in endometrial and colon cancer patients: relationship with tumor progression and metastasis. Voprosy onkologii = Problems in Oncology 2015;61(4):619—23. (In Russ.).

26. Yunusova N.V., Spirina L.V., Frolova A.E. et al. Association of IGFBP-6 expression with metabolic syndrome and adiponectin and IGF-IR receptor levels in colorectal cancer. Asian Pac J Cancer Prev 2016;17(8):3963—9. DOI: 10.22034/APJCP.2016.17.12.5315. PMID: 27644646.

27. Martinez M.C., Andriantsitohaina R. Extracellular Vesicles in Metabolic Syndrome. Circ Res 2017;120(10):1674—86. DOI: 10.1161/CIRCRESA-HA.117.309419.

28. Eitan E., Tosti V., Suire C.N. et al. In a randomized trial in prostate cancer patients, dietary protein restriction modifies markers of leptin and insulin signaling in plasma extracellular vesicles. Aging Cell 2017;16(6):1430—3. DOI 10.1111/acel.12657. PMID: 28921841.

29. Wang J., Wu Y., Guo J. et al. Adipocyte-derived exosomes promote lung cancer metastasis by increasing MMP9 activity via transferring MMP3 to lung cancer cells. Oncotarget 2017;8(47):81880—91. DOI: 10.18632/onco-target.18737. PMID: 29137230.


Review

For citations:


Zambalova E.A., Patysheva M.R., Dimcha A.A., Tamkovich S.N., Grigor’eva A.E., Kolegova E.S., Kondakova I.V., Afanas’ev S.G., Yunusova N.V. Exosomal proteases in colorectal cancer. Advances in Molecular Oncology. 2018;5(4):117-126. (In Russ.) https://doi.org/10.17650/2313-805X-2018-5-4-117-126

Views: 874


Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.


ISSN 2313-805X (Print)
ISSN 2413-3787 (Online)