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Argininosuccinate synthetase (ASS) deficiency in high-grade pulmonary neuroendocrine carcinoma: an opportunity for personalized targeted therapy

  • Original Article – Cancer Research
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Abstract

Purpose

Cells deficient in argininosuccinate synthetase (ASS) must absorb the arginine they need for growth from circulating blood. Treatment with pegylated arginine deiminase (ADI-PEG 20) selectively eliminates arginine from the circulation and has shown some efficacy against ASS-deficient tumors including small cell lung cancer (SCLC). We sought to assess ASS expression in a cohort of high-grade pulmonary neuroendocrine carcinomas (PNEC) which include SCLC and large cell neuroendocrine carcinoma (LCNEC).

Methods

Sixty-nine PNEC (49 SCLC and 20 LCNEC) were retrieved from our pathology archives. Formalin-fixed paraffin-embedded sections of the 54 primary tumors, 15 metastases and appropriate positive and negative controls were immunostained using an ASS-specific monoclonal antibody. Positive staining in <30 % of the tumor was scored as weak; staining in ≥30 % of the tumor was scored as strong. The absence of staining in the tumor was recorded as ASS negative.

Results

58 % of the PNEC including 61.2 % of the SCLC and 50 % of the LCNEC were ASS negative. These ASS-negative tumors included 63 % of the primary and 40 % of the metastatic lesions tested.

Conclusions

More than 50 % of the high-grade PNEC tested lack immunohistochemically detectable ASS, suggesting that they are auxotrophic for arginine and potential candidates for arginine deprivation therapy. PNEC comprise about 25 % of primary lung cancers and have a 5-year overall survival of only 5–10 %, underscoring the need for new and more effective therapies. Immunostaining for ASS has potential to improve the selection of patients with PNEC for arginine deprivation therapy with ADI-PEG 20.

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References

  • Abuchowski A, McCoy JR, Palczuk NC et al (1977a) Effect of covalent attachment of polyethylene glycol on immunogenicity and circulating life of bovine liver catalase. J Biol Chem 252:3582–3586

    PubMed  CAS  Google Scholar 

  • Abuchowski A, van Es T, Palczuk NC et al (1977b) Alteration of immunological properties of bovine serum albumin by covalent attachment of polyethylene glycol. J Biol Chem 252:3578–3581

    PubMed  CAS  Google Scholar 

  • Allen MD, Luong P, Hudson C et al (2014) Prognostic and therapeutic impact of argininosuccinate synthetase 1 control in bladder cancer as monitored longitudinally by PET imaging. Cancer Res 74:896–907

    Article  PubMed  CAS  Google Scholar 

  • Aoun P, Wiggins M, Pickering D et al (2004) Interphase fluorescence in situ hybridization studies for the detection of 9q34 deletions in chronic myelogenous leukemia: a practical approach to clinical diagnosis. Cancer Genet Cytogenet 154:138–143

    Article  PubMed  CAS  Google Scholar 

  • Ascierto PA, Scala S, Castello G et al (2005) Pegylated arginine deiminase treatment of patients with metastatic melanoma: results from phase I and II studies. J Clin Oncol 23:7660–7668

    Article  PubMed  CAS  Google Scholar 

  • Cerami E, Gao J, Dogrusoz U et al (2012) The cBio cancer genomics portal: an open platform for exploring multidimensional cancer genomics data. Cancer Discov 2:401–404

    Article  PubMed  Google Scholar 

  • Cheon DJ, Walts AE, Beach JA et al (2014) Differential expression of ASS1 in serous and non-serous ovarian carcinomas. J Path: Clin Res. doi:10.1002/cjp2.4

    Google Scholar 

  • Davis F (2002) The origin of pegnology. Adv Drug Deliv Rev 54:457–458

    Article  PubMed  CAS  Google Scholar 

  • Ensor CM, Holtsberg FW, Bomalaski JS et al (2002) Pegylated arginine deiminase (ADI-SS PEG20,000 mw) inhibits human melanomas and hepatocellular carcinomas in vitro and in vivo. Cancer Res 62:5443–5450

    PubMed  CAS  Google Scholar 

  • Feun LG, Marini A, Walker G et al (2012) Negative argininosuccinate synthetase expression in melanoma tumours may predict clinical benefit from arginine-depleting therapy with pegylated arginine deiminase. Br J Cancer 106:1481–1485

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  • Fontenelle LJ, Henderson JF (1969) Sources of nitrogen as rate-limiting factors for purine biosynthesis de novo in Ehrlich ascites tumor cells. Biochim Biophys Acta 177:88–93

    Article  PubMed  CAS  Google Scholar 

  • Gao J, Aksoy BA, Dogrusoz U et al (2013) Integrative analysis of complex cancer genomics and clinical profiles using the cBioPortal. Sci Signal. 6:l1

    Article  Google Scholar 

  • Haines RJ (2011) PendletonLC, Eichler DC. Argininosuccinate synthetase: at the center of arginine metabolism. Int J Biochem Mol Biol 2:8–23

    PubMed  CAS  PubMed Central  Google Scholar 

  • He W, Chen J, Zheng Y et al (2010) Lack of expression of arginionosuccinate synthetase in human cancer tissue: a biomarker for sensitivity to arginine depletion with pegylated arginine deiminase [abstract]. In: Proceedings of the 101st annual meeting of the American Association for Cancer Research, Apr 17–21; Washington, DC: AACR; 2010. Abstract #4703

  • Huang H-Y, Wu W-R, Wang Y-H et al (2013) ASS1 as a novel tumor suppressor gene in myxofibrosarcomas: aberrant loss via epigenetic DNA methylation confers aggressive phenotypes, negative prognostic impact, and therapeutic relevance. Clin Cancer Res 19:2861–2872

    Article  PubMed  CAS  Google Scholar 

  • Izzo F, Marra P, Beneduce G et al (2004) Pegylated arginine deiminase treatment of patients with unresectable hepatocellular carcinoma: results from phase I/II studies. J Clin Oncol 22:1815–1822

    Article  PubMed  CAS  Google Scholar 

  • Jungbluth A, Tassello J, Frosina D et al (2010) Expression pattern of argininosuccinate-synthetase (ASS) in normal and tumor tissue as a marker for susceptibility to arginine-deiminase (ADI) therapy. Mod Pathol 23(Suppl1):387A

    Google Scholar 

  • Kelly MP, Jungbluth AA, Wu BW et al (2012) Arginine deiminase PEG20 inhibits growth of small cell lung cancers lacking expression of argininosuccinate synthetase. Br J Cancer 106:324–332

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  • Lan J, Tai HC, Lee SW et al (2014) Deficiency in expression and epigenetic DNA methylation of ASS1 gene in nasopharyngeal carcinoma: negative prognostic impact and therapeutic relevance. Tumour Biol 35:161–169

    Article  PubMed  CAS  Google Scholar 

  • Long Y, Tsai WB, Wangpaichitr M et al (2013) Arginine deiminase resistance in melanoma cells is associated with metabolic reprogramming, glucose dependence, and glutamine addiction. Mol Cancer Ther 12:2581–2590

    Article  PubMed  CAS  Google Scholar 

  • Phillips MM, Sheaff MT, Szlosarek PW (2013) Targeting arginine-dependent cancers with arginine-degrading enzymes: opportunities and challenges. Cancer Res Treat 45:251–262

    Article  PubMed  PubMed Central  Google Scholar 

  • Qiu F, Chen YR, Liu X et al (2004) (2104) Arginine starvation impairs mitochondrial respiratory function in ASS1-deficient breast cancer cells. Sci Signal 7(319):ra31. doi:10.1126/scisignal761

    Article  Google Scholar 

  • Shen LJ, Lin WC, Beloussow K, Shen WC (2003) Resistance to the anti-proliferative activity of recombinant arginine deiminase in cell culture correlates with the endogenous enzyme, argininosuccinate synthetase. Cancer Lett 191:165–170

    Article  PubMed  CAS  Google Scholar 

  • Syed N, O’Neill K, Highes M et al (2011) Transcriptional silencing disrupts two levels of arginine biosynthesis in glioblastoma multiforme: a novel, targeted therapeutic strategy for high grade gliomas [abstract]. In: In: Proceedings of the 102nd annual meeting of the American Association for Cancer Research; 2011 Apr 2–6; Orlando, FL: AACR. Abstract #LB260

  • Synakiewicz A, Stachowicz-Stencel T, Adamkiewicz-Drozynska E (2014) The role of arginine and the modified arginine deiminase enzyme ADI-PEG 20 in cancer therapy with special emphasis on Phase I/II clinical trials. Expert Opin Investig Drugs 23:1–13

    Article  Google Scholar 

  • Szlosarek PW, Luong F, Clear A et al (2011) Pegylated aqrginine deiminase (ADI-PEG20) as a potential novel therapy for argininosuccinate synthetase-deficient acute myeloid leukemia. [abstract]. In: Proceedings of the 102nd annual meeting of the American Association for Cancer Research, Apr 2–6; Orlando, FL: AACR; 2011. Abstract #4067

  • Szlosarek PW, Steele JP, Nolan L et al (2014) Randomized trial of arginine deprivation with pegylated arginine deiminase in patients with malignant pleural mesothelioma. J Clin Oncol 32:5s (suppl; abstr 7507)

  • Szlosarek PW, Klabatsa A, Pallaska A et al (2006) In vivo loss of expression of argininosuccinate synthetase in malignant pleural mesothelioma is a biomarker for susceptibility to arginine depletion. Clin Cancer Res 12:7126–7131

    Article  PubMed  CAS  Google Scholar 

  • Szlosarek PW, Luong P, Phillips MM et al (2013) Metabolic response to pegylated arginine deiminase in mesothelioma with promoter methylation of argininosuccinate synthetase. J Clin Oncol 31:e111–e113

    Article  PubMed  Google Scholar 

  • Weich D, Li S, Kitchens T et al (2012) Arginine depravation therapy with arginine deiminase and autopohagy inhibition is a novel therapeutic approach for the treatment of metastatic sarcomas that lack argininosuccinate synthetsase expression [abstract]. In: Proceedings of the 103rd annual meeting of the American Association for Cancer Research, 2012 Mar 31–Apr 4; Chicago, IL: AACR; 2012. Abstract #5629

  • www.cancer.gov/cancertopics [Web site]. http://www.cancer.gov/cancertopics.Accessed Oct 21, 2014

  • www.cbioportal [website]. http://www.cbioportal. Accessed Oct 20, 2014

  • www.clinicaltrials.gov [Web site]. http://www.clinicaltrials.gov. Accessed Oct 20, 2014

  • www.SEER.cancer.gov/statfacts/html/lungb.html [Web site]. http://www.SEER.cancer.gov/statfacts/html/lungb.html. Accessed Oct 21, 2014

  • Yang T-S, Lu S-N, Chao et al (2010) A randomized phase II study of pegylated arginine deiminase (ADI-PEG 20) in Asian advanced hepatocellular carcinoma patients. Br J Cancer 103:954–960

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  • Yoon CY, Shim YJ, Kim EH et al (2007) Renal cell carcinoma does not express argininosuccinate synthetase and is highly sensitive to arginine deprivation via arginine deiminase. Int J Cancer 120:897–905

    Article  PubMed  CAS  Google Scholar 

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Conflict of interest

JSB is a stock owner and employee of the Polaris Group, Inc., which produces ADI-PEG 20. Other authors declare no conflicts of interest.

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Correspondence to Ann E. Walts.

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Walts, A.E., Bomalaski, J.S., Ines, D. et al. Argininosuccinate synthetase (ASS) deficiency in high-grade pulmonary neuroendocrine carcinoma: an opportunity for personalized targeted therapy. J Cancer Res Clin Oncol 141, 1363–1369 (2015). https://doi.org/10.1007/s00432-014-1904-z

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  • DOI: https://doi.org/10.1007/s00432-014-1904-z

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