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Erschienen in: Clinical and Translational Oncology 7/2019

18.12.2018 | Research Article

High calpain-1 expression predicts a poor clinical outcome and contributes to tumor progression in pancreatic cancer patients

verfasst von: L. M. Yu, Y. S. Zhu, C. Z. Xu, L. L. Zhou, Z. X. Xue, Z. Z. Cai

Erschienen in: Clinical and Translational Oncology | Ausgabe 7/2019

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Abstract

Background

Pancreatic cancer (PC) is a highly aggressive and metastatic disease, with an elevated mortality rate. It is, therefore, crucial to assess factors affecting the prognosis of PC patients. Meanwhile, calpain-1 is associated with malignant tumor progression and metastasis. Thus, it is meaningful to evaluate the relationship between calpain-1 and PC.

Materials and methods

Calpain-1 protein expression was assessed by immunohistochemistry in 96 pancreatic cancer samples and paired adjacent non-cancerous specimens. In addition, calpain-1 protein levels were assessed in six PC cell lines by western blot (WB). Next, PC cells were transfected with calpain-1 siRNA, and silencing was confirmed by WB. Finally, cell proliferation, colony formation, migration and invasion assays, and cell apoptosis analysis were performed to examine the effects of calpain-1 knockdown on proliferation, growth, apoptosis, migration, and invasion in PC cells.

Results

The results showed that calpain-1 was overexpressed in PC tissues and cells. Meanwhile, calpain-1 overexpression was associated with tumor site (P = 0.029), metastasis (P = 0.000), and TNM stage (P = 0.000), but showed no associations with histological grade (P = 0.396), age (P = 0.809), sex (P = 1.000), and lesion size (P = 0.679). The Kaplan–Meier method demonstrated that the low calpain-1 expression group had increased overall survival (OS) compared with patients expressing high calpain-1 levels (28.7 ± 4.1 vs. 17.0 ± 2.3 months) (P = 0.005). Besides, calpain-1 in PC cells was successfully silenced by liposome-mediated RNA interference, resulting in reduced cell growth, invasion, and metastasis in PC cells, with no effect on apoptosis.

Conclusion

The above findings suggest that calpain-1 should be considered a potential biomarker for PC prognosis and therapy.
Literatur
4.
Zurück zum Zitat Ryan DP, Hong TS, Bardeesy N. Pancreatic Adenocarcinoma. New Engl J Med. 2014;371(11):1039–49.CrossRefPubMed Ryan DP, Hong TS, Bardeesy N. Pancreatic Adenocarcinoma. New Engl J Med. 2014;371(11):1039–49.CrossRefPubMed
5.
Zurück zum Zitat Goll DE, Thompson VF, Li HQ, Wei W, Cong JY. The calpain system. Physiol Rev. 2003;83(3):731–801.CrossRefPubMed Goll DE, Thompson VF, Li HQ, Wei W, Cong JY. The calpain system. Physiol Rev. 2003;83(3):731–801.CrossRefPubMed
6.
Zurück zum Zitat Storr SJ, Carragher NO, Frame MC, Parr T, Martin SG. The calpain system and cancer. Nat Rev Cancer. 2011;11(5):364–74.CrossRefPubMed Storr SJ, Carragher NO, Frame MC, Parr T, Martin SG. The calpain system and cancer. Nat Rev Cancer. 2011;11(5):364–74.CrossRefPubMed
7.
Zurück zum Zitat Potz BA, Abid MR, Sellke FW. Role of calpain in pathogenesis of human disease processes. J Nat Sci. 2016;2(9):e218.PubMedPubMedCentral Potz BA, Abid MR, Sellke FW. Role of calpain in pathogenesis of human disease processes. J Nat Sci. 2016;2(9):e218.PubMedPubMedCentral
8.
Zurück zum Zitat Carragher NO, Frame MC. Calpain: a role in cell transformation and migration. Int J Biochem Cell B. 2002;34(12):1539–43.CrossRef Carragher NO, Frame MC. Calpain: a role in cell transformation and migration. Int J Biochem Cell B. 2002;34(12):1539–43.CrossRef
9.
Zurück zum Zitat Reichrath J, Welter C, Mitschele T, et al. Different expression patterns of calpain isozymes 1 and 2 (CAPN1 and 2) in squamous cell carcinomas (SCC) and basal cell carcinomas (BCC) of human skin. J Pathol. 2003;199(4):509–16.CrossRefPubMed Reichrath J, Welter C, Mitschele T, et al. Different expression patterns of calpain isozymes 1 and 2 (CAPN1 and 2) in squamous cell carcinomas (SCC) and basal cell carcinomas (BCC) of human skin. J Pathol. 2003;199(4):509–16.CrossRefPubMed
10.
Zurück zum Zitat Leloup L, Wells A. Calpains as potential anti-cancer targets. Expert Opin Ther Tar. 2011;15(3):309–23.CrossRef Leloup L, Wells A. Calpains as potential anti-cancer targets. Expert Opin Ther Tar. 2011;15(3):309–23.CrossRef
11.
Zurück zum Zitat Ma D, Fang J, Liu Y, et al. High level of calpain1 promotes cancer cell invasion and migration in oral squamous cell carcinoma. Oncol Lett. 2017;13(6):4017–26.CrossRefPubMedPubMedCentral Ma D, Fang J, Liu Y, et al. High level of calpain1 promotes cancer cell invasion and migration in oral squamous cell carcinoma. Oncol Lett. 2017;13(6):4017–26.CrossRefPubMedPubMedCentral
12.
Zurück zum Zitat Al-Bahlani SM, Al-Rashdi RM, Kumar S, Al-Sinawi SS, Al-Bahri MA, Shalaby AA. Calpain-1 expression in triple-negative breast cancer: a potential prognostic factor independent of the proliferative/apoptotic index. Biomed Res Int. 2017;2017:9290425.PubMedPubMedCentral Al-Bahlani SM, Al-Rashdi RM, Kumar S, Al-Sinawi SS, Al-Bahri MA, Shalaby AA. Calpain-1 expression in triple-negative breast cancer: a potential prognostic factor independent of the proliferative/apoptotic index. Biomed Res Int. 2017;2017:9290425.PubMedPubMedCentral
13.
Zurück zum Zitat Luo W, Ren Z, Gao S, et al. Clinical correlation of calpain-1 and glypican-3 expression with gallbladder carcinoma. Oncol Lett. 2016;11(2):1345–52.CrossRefPubMedPubMedCentral Luo W, Ren Z, Gao S, et al. Clinical correlation of calpain-1 and glypican-3 expression with gallbladder carcinoma. Oncol Lett. 2016;11(2):1345–52.CrossRefPubMedPubMedCentral
14.
Zurück zum Zitat Yoshida M, Miyasaka Y, Ohuchida K, et al. Calpain inhibitor calpeptin suppresses pancreatic cancer by disrupting cancer-stromal interactions in a mouse xenograft model. Cancer Sci. 2016;107(10):1443–52.CrossRefPubMedPubMedCentral Yoshida M, Miyasaka Y, Ohuchida K, et al. Calpain inhibitor calpeptin suppresses pancreatic cancer by disrupting cancer-stromal interactions in a mouse xenograft model. Cancer Sci. 2016;107(10):1443–52.CrossRefPubMedPubMedCentral
15.
Zurück zum Zitat Guroff G. A neutral, calcium-activated proteinase from the soluble fraction of rat brain. J Biol Chem. 1964;239:149–55.PubMed Guroff G. A neutral, calcium-activated proteinase from the soluble fraction of rat brain. J Biol Chem. 1964;239:149–55.PubMed
16.
Zurück zum Zitat Huttenlocher A, Palecek SP, Lu Q, et al. Regulation of cell migration by the calcium-dependent protease calpain. J Biol Chem. 1997;272(52):32719–22.CrossRefPubMed Huttenlocher A, Palecek SP, Lu Q, et al. Regulation of cell migration by the calcium-dependent protease calpain. J Biol Chem. 1997;272(52):32719–22.CrossRefPubMed
17.
Zurück zum Zitat Braun C, Engel M, Seifert M, et al. Expression of calpain I messenger RNA in human renal cell carcinoma: correlation with lymph node metastasis and histological type. Int J Cancer. 1999;84(1):6–9.CrossRefPubMed Braun C, Engel M, Seifert M, et al. Expression of calpain I messenger RNA in human renal cell carcinoma: correlation with lymph node metastasis and histological type. Int J Cancer. 1999;84(1):6–9.CrossRefPubMed
18.
Zurück zum Zitat Starska K, Forma E, Jozwiak P, et al. Gene/protein expression of CAPN1/2-CAST system members is associated with ERK1/2 kinases activity as well as progression and clinical outcome in human laryngeal cancer. Tumor Biol. 2016;37(10):13185–203.CrossRef Starska K, Forma E, Jozwiak P, et al. Gene/protein expression of CAPN1/2-CAST system members is associated with ERK1/2 kinases activity as well as progression and clinical outcome in human laryngeal cancer. Tumor Biol. 2016;37(10):13185–203.CrossRef
19.
Zurück zum Zitat Liu BD, Zhou Y, Lu D, et al. Comparison of the protein expression of calpain-1, calpain-2, calpastatin and calmodulin between gastric cancer and normal gastric mucosa. Oncol Lett. 2017;14(3):3705–10.CrossRefPubMedPubMedCentral Liu BD, Zhou Y, Lu D, et al. Comparison of the protein expression of calpain-1, calpain-2, calpastatin and calmodulin between gastric cancer and normal gastric mucosa. Oncol Lett. 2017;14(3):3705–10.CrossRefPubMedPubMedCentral
20.
Zurück zum Zitat Storr SJ, Pu X, Davis J, et al. Expression of the calpain system is associated with poor clinical outcome in gastro-oesophageal adenocarcinomas. J Gastroenterol. 2013;48(11):1213–21.CrossRefPubMed Storr SJ, Pu X, Davis J, et al. Expression of the calpain system is associated with poor clinical outcome in gastro-oesophageal adenocarcinomas. J Gastroenterol. 2013;48(11):1213–21.CrossRefPubMed
21.
Zurück zum Zitat Demarchi F, Schneider C. The calpain system as a modulator of stress/damage response. Cell Cycle. 2007;6(2):136–8.CrossRefPubMed Demarchi F, Schneider C. The calpain system as a modulator of stress/damage response. Cell Cycle. 2007;6(2):136–8.CrossRefPubMed
22.
Zurück zum Zitat Burrows F, Zhang H, Kamal A. Hsp90 activation and cell cycle regulation. Cell Cycle. 2004;3(12):1530–6.CrossRefPubMed Burrows F, Zhang H, Kamal A. Hsp90 activation and cell cycle regulation. Cell Cycle. 2004;3(12):1530–6.CrossRefPubMed
23.
Zurück zum Zitat Mlynarczuk-Bialy I, Roeckmann H, Kuckelkorn U, et al. Combined effect of proteasome and calpain inhibition on cisplatin-resistant human melanoma cells. Cancer Res. 2006;66(15):7598–605.CrossRefPubMed Mlynarczuk-Bialy I, Roeckmann H, Kuckelkorn U, et al. Combined effect of proteasome and calpain inhibition on cisplatin-resistant human melanoma cells. Cancer Res. 2006;66(15):7598–605.CrossRefPubMed
24.
Zurück zum Zitat Kassis J, Radinsky R, Wells A. Motility is rate-limiting for invasion of bladder carcinoma cell lines. Int J Biochem Cell B. 2002;34(7):762–75.CrossRef Kassis J, Radinsky R, Wells A. Motility is rate-limiting for invasion of bladder carcinoma cell lines. Int J Biochem Cell B. 2002;34(7):762–75.CrossRef
Metadaten
Titel
High calpain-1 expression predicts a poor clinical outcome and contributes to tumor progression in pancreatic cancer patients
verfasst von
L. M. Yu
Y. S. Zhu
C. Z. Xu
L. L. Zhou
Z. X. Xue
Z. Z. Cai
Publikationsdatum
18.12.2018
Verlag
Springer International Publishing
Erschienen in
Clinical and Translational Oncology / Ausgabe 7/2019
Print ISSN: 1699-048X
Elektronische ISSN: 1699-3055
DOI
https://doi.org/10.1007/s12094-018-02006-6

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