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Dipeptidyl Peptidase 9 Increases Chemoresistance and is an Indicator of Poor Prognosis in Colorectal Cancer

  • Translational Research and Biomarkers
  • Published:
Annals of Surgical Oncology Aims and scope Submit manuscript

Abstract

Background

In recent years, systemic chemotherapy has significantly improved the prognosis of metastatic colorectal cancer (CRC); however, different patients have different responses to chemotherapeutics.

Methods

Dipeptidyl peptidase 9 (DPP9) is an enzyme in the dipeptidyl peptidase IV family that has been reported to increase drug sensitivity in acute myeloid leukemia. In this study, we examined the relationship between DPP9 expression and the prognosis of patients with CRC, as well as the role of DPP9 in anticancer drug resistance. Moreover, the effects of the DPP9 inhibitors talabostat and vildagliptin in CRC cell lines and primary cultured cells were assessed.

Results

High expression of DPP9 was associated with worse prognosis in 196 patients with CRC. Cell viability was markedly inhibited in CRC cell lines transfected with DPP9 small interfering RNA or small hairpin RNA. Talabostat suppressed proliferation in CRC cell lines and primary cultured cells, and increased their sensitivity to chemotherapy. Vildagliptin, a DPP family inhibitor currently administered for diabetes, also increased the sensitivity of CRC cells to anticancer drugs.

Conclusion

DPP9 was a poor prognostic factor for CRC and could be a new therapeutic target, while vildagliptin could be used as a repositioned drug for CRC treatment.

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References

  1. Siegel RL, Miller KD, Jemal A. Cancer statistics, 2018. CA Cancer J Clin. 2018;68:7–30.

    PubMed  Google Scholar 

  2. Matsuda T, Yamashita K, Hasegawa H, Oshikiri T, Hosono M, Higashino N, et al. Recent updates in the surgical treatment of colorectal cancer. Ann Gastroenterol Surg. 2018;2:129–36.

    PubMed  PubMed Central  Google Scholar 

  3. Grothey A, Sargent D, Goldberg RM, Schmoll HJ. Survival of patients with advanced colorectal cancer improves with the availability of fluorouracil–leucovorin, irinotecan, and oxaliplatin in the course of treatment. J Clin Oncol. 2004;22:1209–14.

    CAS  PubMed  Google Scholar 

  4. Hurwitz H, Fehrenbacher L, Novotny W, Cartwright T, Hainsworth J, Heim W, et al. Bevacizumab plus irinotecan, fluorouracil, and leucovorin for metastatic colorectal cancer. N Engl J Med. 2004;350:2335–42.

    CAS  PubMed  Google Scholar 

  5. Sobrero AF, Maurel J, Fehrenbacher L, Scheithauer W, Abubakr YA, Lutz MP, et al. EPIC: phase III trial of cetuximab plus irinotecan after fluoropyrimidine and oxaliplatin failure in patients with metastatic colorectal cancer. J Clin Oncol. 2008;26:2311–19.

    CAS  PubMed  Google Scholar 

  6. Ajami K, Abbott CA, McCaughan GW, Gorrell MD. Dipeptidyl peptidase 9 has two forms, a broad tissue distribution, cytoplasmic localization and DPIV-like peptidase activity. Biochim Biophys Acta. 2004;1679:18–28.

    CAS  PubMed  Google Scholar 

  7. Abbott CA, Yu DM, Woollatt E, Sutherland GR, McCaughan GW, Gorrell MD. Cloning, expression and chromosomal localization of a novel human dipeptidyl peptidase (DPP) IV homolog, DPP8. Eur J Biochem. 2000;267:6140–50.

    CAS  PubMed  Google Scholar 

  8. Olsen C, Wagtmann N. Identification and characterization of human DPP9, a novel homologue of dipeptidyl peptidase IV. Gene. 2002;299:185–93.

    CAS  PubMed  Google Scholar 

  9. Rummey C, Metz G. Homology models of dipeptidyl peptidases 8 and 9 with a focus on loop predictions near the active site. Proteins. 2007;66:160–71.

    CAS  PubMed  Google Scholar 

  10. Qi SY, Riviere PJ, Trojnar J, Junien JL, Akinsanya KO. Cloning and characterization of dipeptidyl peptidase 10, a new member of an emerging subgroup of serine proteases. Biochem J. 2003;373:179–89.

    CAS  PubMed  PubMed Central  Google Scholar 

  11. Pitman MR, Sulda ML, Kuss B, Abbott CA. Dipeptidyl peptidase 8 and 9—guilty by association? Front Biosci (Landmark Ed). 2009;14:3619–33.

    CAS  Google Scholar 

  12. Zhang H, Chen Y, Keane FM, Gorrell MD. Advances in understanding the expression and function of dipeptidyl peptidase 8 and 9. Mol Cancer Res. 2013;11:1487–96.

    CAS  PubMed  Google Scholar 

  13. Johnson DC, Taabazuing CY, Okondo MC, Chui AJ, Rao SD, Brown FC, et al. DPP8/DPP9 inhibitor-induced pyroptosis for treatment of acute myeloid leukemia. Nat Med. 2018;24:1151–56.

    CAS  PubMed  PubMed Central  Google Scholar 

  14. Tang Z, Li J, Shen Q, Feng J, Liu H, Wang W, et al. Contribution of upregulated dipeptidyl peptidase 9 (DPP9) in promoting tumoregenicity, metastasis and the prediction of poor prognosis in non-small cell lung cancer (NSCLC). Int J Cancer. 2017;140:1620–32.

    CAS  PubMed  PubMed Central  Google Scholar 

  15. Smebye ML, Agostini A, Johannessen B, Thorsen J, Davidson B, Trope CG, et al. Involvement of DPP9 in gene fusions in serous ovarian carcinoma. BMC Cancer. 2017;17:642.

    PubMed  PubMed Central  Google Scholar 

  16. Lankas GR, Leiting B, Roy RS, Eiermann GJ, Beconi MG, Biftu T, et al. Dipeptidyl peptidase IV inhibition for the treatment of type 2 diabetes: potential importance of selectivity over dipeptidyl peptidases 8 and 9. Diabetes. 2005;54:2988–94.

    CAS  PubMed  Google Scholar 

  17. Jiaang WT, Chen YS, Hsu T, Wu SH, Chien CH, Chang CN, et al. Novel isoindoline compounds for potent and selective inhibition of prolyl dipeptidase DPP8. Bioorg Med Chem Lett. 2005;15:687–91.

    CAS  PubMed  Google Scholar 

  18. Waumans Y, Baerts L, Kehoe K, Lambeir AM, De Meester I. The dipeptidyl peptidase family, prolyl oligopeptidase, and prolyl carboxypeptidase in the immune system and inflammatory disease, including atherosclerosis. Front Immunol. 2015;6:387.

    PubMed  Google Scholar 

  19. Mari A, Sallas WM, He YL, Watson C, Ligueros-Saylan M, Dunning BE, et al. Vildagliptin, a dipeptidyl peptidase-IV inhibitor, improves model-assessed beta-cell function in patients with type 2 diabetes. J Clin Endocrinol Metab. 2005;90:4888–94.

    CAS  PubMed  Google Scholar 

  20. Burkey BF, Hoffmann PK, Hassiepen U, Trappe J, Juedes M, Foley JE. Adverse effects of dipeptidyl peptidases 8 and 9 inhibition in rodents revisited. Diabetes Obes Metab. 2008;10:1057–61.

    CAS  PubMed  Google Scholar 

  21. Amritha CA, Kumaravelu P, Chellathai DD. Evaluation of anti cancer effects of DPP-4 inhibitors in colon cancer—an invitro Study. J Clin Diagn Res. 2015;9:FC14–6.

    CAS  PubMed  PubMed Central  Google Scholar 

  22. Spagnuolo PA, Hurren R, Gronda M, MacLean N, Datti A, Basheer A, et al. Inhibition of intracellular dipeptidyl peptidases 8 and 9 enhances parthenolide’s anti-leukemic activity. Leukemia. 2013;27:1236–44.

    CAS  PubMed  Google Scholar 

  23. Watanabe T, Muro K, Ajioka Y, Hashiguchi Y, Ito Y, Saito Y, et al. Japanese Society for Cancer of the Colon and Rectum (JSCCR) guidelines 2016 for the treatment of colorectal cancer. Int J Clin Oncol. 2018;23:1–34.

    PubMed  Google Scholar 

  24. Fujino S, Ito A, Ohue M, Yasui M, Mizushima T, Doki Y, et al. Phenotypic heterogeneity of 2D organoid reflects clinical tumor characteristics. Biochem Biophys Res Commun. 2019;513:332–9.

    CAS  PubMed  Google Scholar 

  25. Sikandar SS, Pate KT, Anderson S, Dizon D, Edwards RA, Waterman ML et al. NOTCH signaling is required for formation and self-renewal of tumor-initiating cells and for repression of secretory cell differentiation in colon cancer. Cancer Res. 2010;70(4):1469–78.

  26. Fujino S, Myoshi N, Saso K, Sasaki M, Ishikawa S, Takahashi Y, et al. The inflammation-nutrition score supports the prognostic prediction of the TNM stage for colorectal cancer patients after curative resection. Surg Today. 2020;50(2):163–70.

    CAS  PubMed  Google Scholar 

  27. Yao TW, Kim WS, Yu DM, Sharbeen G, McCaughan GW, Choi KY, et al. A novel role of dipeptidyl peptidase 9 in epidermal growth factor signaling. Mol Cancer Res. 2011;9:948–59.

    CAS  PubMed  Google Scholar 

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Acknowledgment

The authors would like to thank Ms. Aya Ito for special technical assistance regarding sample preparation.

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Authors

Corresponding author

Correspondence to Norikatsu Miyoshi MD, PhD, FICS, FACS.

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Disclosure

Kazuhiro Saso, Norikatsu Myoshi, Shiki Fujino, Masaru Sasaki, Masayoshi Yasui, Masayuki Ohue, Takayuki Ogino, Hidekazu Takahashi, Mamoru Uemura, Chu Matsuda, Tsunekazu Mizushima, Yuichiro Doki, and Hidetoshi Eguchi declare no competing financial interests.

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10434_2020_8729_MOESM1_ESM.png

Supplementary Figure 1 Violin plots depicting the median DPP9/GAPDH ratio in 196 CRC patients based on stage. There were no significant differences based on stage (P = 0.940). DPP9, dipeptidyl peptidase 9; GAPDH; glyceraldehyde-3-phosphate dehydrogenase; CRC: colorectal cancer (PNG 122 kb)

10434_2020_8729_MOESM2_ESM.png

Supplementary Figure 2 Postoperative disease-free survival rates in patients with high and low DPP9 expression were not significantly different. DPP9, dipeptidyl peptidase 9; GAPDH; glyceraldehyde-3-phosphate dehydrogenase (PNG 153 kb)

10434_2020_8729_MOESM3_ESM.png

Supplementary Figure 3 Overall survival based on DPP9 mRNA expression in CRC patients with postoperative recurrence. The 5-year OS was lower in patients with high DPP9 expression compared to those with low expression. DPP9, dipeptidyl peptidase 9; GAPDH; glyceraldehyde-3-phosphate dehydrogenase; CRC, colorectal cancer; OS, overall survival (PNG 170 kb)

10434_2020_8729_MOESM4_ESM.png

Supplementary Figure 4 DPP9 expression is increased in CRC and high expression is associated with worse overall survival in patients with adjuvant chemotherapy. In patient who were treated by adjuvant chemotherapy, the high-expression group had significantly lower 5-years OS than the low-expression group (P = 0.034), but there is no significant difference in disease-free survival between the two groups (P = 0.428). DPP9, dipeptidyl peptidase 9; GAPDH; glyceraldehyde-3-phosphate dehydrogenase; CRC, colorectal cancer; OS, overall survival (PNG 103 kb)

10434_2020_8729_MOESM5_ESM.png

Supplementary Figure 5 In patient who had recurrence and were treated by chemotherapy, the high-expression group had lower OS than the low-expression group (P = 0.067). DPP9, dipeptidyl peptidase 9; GAPDH; glyceraldehyde-3-phosphate dehydrogenase; CRC: colorectal cancer; OS, overall survival (PNG 135 kb)

Supplementary material 6 (XLSX 9 kb)

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Saso, K., Miyoshi, N., Fujino, S. et al. Dipeptidyl Peptidase 9 Increases Chemoresistance and is an Indicator of Poor Prognosis in Colorectal Cancer. Ann Surg Oncol 27, 4337–4347 (2020). https://doi.org/10.1245/s10434-020-08729-7

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  • DOI: https://doi.org/10.1245/s10434-020-08729-7

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