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Published in: Head and Neck Pathology 4/2020

01-12-2020 | Case Reports

HDAC Overexpression in a NUT Midline Carcinoma of the Parotid Gland with Exceptional Survival: A Case Report

Authors: Gonçalo Esteves, Joana Ferreira, Rita Afonso, Carmo Martins, Carlos Zagalo, Ana Félix

Published in: Head and Neck Pathology | Issue 4/2020

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Abstract

NUT midline carcinoma (NMC) is a recently described entity with a predilection for young individuals, characterised by a rearrangement of NUT, most commonly with BRD4. It usually involves midline structures, with a minority of cases presenting outside the midline axis. Given its dismal prognosis, new molecularly targeted therapies (eg, HDAC inhibitors) are gaining ground, but the HDAC expression pattern remains unknown. We describe the exceptional evolution of a NMC arising in the parotid gland. A 34-year-old male presented with a rapidly growing 35 mm left-parotid mass. Parotidectomy and lymphadenectomy were performed. The tumour invaded the surrounding soft tissue and lay adjacent to the surgical margin. No lymph node metastases were identified. Histology revealed blue nests of undifferentiated cells merging with foci of necrosis and occasional abrupt foci of keratinising squamous epithelium. FISH analysis confirmed a rearrangement of NUT, but not of BRD4. A diagnosis of NMC was rendered. Currently, after adjuvant chemoradiotherapy and 47 months after diagnosis, the patient is alive and well. The tumour was found to have increased immunoexpression of HDAC2, 4 and 6 and phospho-HDAC4/5/7. This case emphasises the importance of considering NMC in the differential diagnosis of poorly differentiated carcinomas of the head and neck region in young adults, even away from midline structures. As molecular targets hold the promise of successful therapy for the vast majority of NMC patients, the knowledge of their HDAC expression patterns will probably be relevant.
Literature
1.
go back to reference Giridhar P, Mallick S, Kashyap L, et al. Patterns of care and impact of prognostic factors in the outcome of NUT midline carcinoma: a systematic review and individual patient data analysis of 119 cases. Eur Arch Otorhinolaryngol. 2018;275(3):815–21.CrossRef Giridhar P, Mallick S, Kashyap L, et al. Patterns of care and impact of prognostic factors in the outcome of NUT midline carcinoma: a systematic review and individual patient data analysis of 119 cases. Eur Arch Otorhinolaryngol. 2018;275(3):815–21.CrossRef
2.
go back to reference Bauer DE, Mitchell CM, Strait KM, et al. Clinicopathologic features and long-term outcomes of NUT midline carcinoma. Clin Cancer Res. 2012;18(20):5773–9.CrossRef Bauer DE, Mitchell CM, Strait KM, et al. Clinicopathologic features and long-term outcomes of NUT midline carcinoma. Clin Cancer Res. 2012;18(20):5773–9.CrossRef
3.
go back to reference French CA. Demystified molecular pathology of NUT midline carcinomas. J Clin Pathol. 2008;63:492–6.CrossRef French CA. Demystified molecular pathology of NUT midline carcinomas. J Clin Pathol. 2008;63:492–6.CrossRef
4.
go back to reference French CA, Kutok JL, Faquin WC, et al. Midline carcinoma of children and young adults with NUT rearrangement. J Clin Oncol. 2004;22:4135–9.CrossRef French CA, Kutok JL, Faquin WC, et al. Midline carcinoma of children and young adults with NUT rearrangement. J Clin Oncol. 2004;22:4135–9.CrossRef
5.
go back to reference Samples S, Gleditsch K, Polimenakos A. Intrapericardial NUT midline carcinoma: unusual presentation of a rare tumor and literature review with management considerations. Pediatr Cardiol. 2016;37:208–11.CrossRef Samples S, Gleditsch K, Polimenakos A. Intrapericardial NUT midline carcinoma: unusual presentation of a rare tumor and literature review with management considerations. Pediatr Cardiol. 2016;37:208–11.CrossRef
6.
go back to reference Shehata BM, Steelman CK, Abranowsky CR, et al. NUT midline carcinoma in a newborn with multiorgan disseminated tumor and a 2-year-old with a pancreatic/hepatic primary. Pediatr Dev Pathol. 2010;13:481–5.CrossRef Shehata BM, Steelman CK, Abranowsky CR, et al. NUT midline carcinoma in a newborn with multiorgan disseminated tumor and a 2-year-old with a pancreatic/hepatic primary. Pediatr Dev Pathol. 2010;13:481–5.CrossRef
7.
go back to reference Den Bakker MA, Beverloo BH, van den Heuvel-Eibrink MM, et al. NUT midline carcinoma of the parotid gland with mesenchymal differentiation. Am J Surg Pathol. 2009;33:1253–8.CrossRef Den Bakker MA, Beverloo BH, van den Heuvel-Eibrink MM, et al. NUT midline carcinoma of the parotid gland with mesenchymal differentiation. Am J Surg Pathol. 2009;33:1253–8.CrossRef
8.
go back to reference Ziai J, French CA, Zambrano E. NUT gene rearrangement in a poorly differentiated carcinoma of the submandibular gland. Head Neck Pathol. 2010;4:163–8.CrossRef Ziai J, French CA, Zambrano E. NUT gene rearrangement in a poorly differentiated carcinoma of the submandibular gland. Head Neck Pathol. 2010;4:163–8.CrossRef
9.
go back to reference Park HS, Bae YS, Yoon SO, et al. Usefulness of nuclear protein in testis (NUT) immunohistochemistry in the cytodiagnosis of NUT midline carcinoma: a brief case report. Korean J Pathol. 2014;48:335–8.CrossRef Park HS, Bae YS, Yoon SO, et al. Usefulness of nuclear protein in testis (NUT) immunohistochemistry in the cytodiagnosis of NUT midline carcinoma: a brief case report. Korean J Pathol. 2014;48:335–8.CrossRef
10.
go back to reference Klijanienko J, Le Tourneau C, Rodriguez J, et al. Cytological features of NUT midline carcinoma arising in sino-nasal tract and parotid gland: report of two new cases and review of the literature. Diagn Cytopathol. 2016;44:753–6.CrossRef Klijanienko J, Le Tourneau C, Rodriguez J, et al. Cytological features of NUT midline carcinoma arising in sino-nasal tract and parotid gland: report of two new cases and review of the literature. Diagn Cytopathol. 2016;44:753–6.CrossRef
11.
go back to reference Vulsteke C, Lurquin E, Debiec-Rychter M, et al. First evidence of treatment efficacy in metastatic carcinoma of the parotid gland with BRD4/NUT translocation. J Chemother. 2016;28(3):242–6.CrossRef Vulsteke C, Lurquin E, Debiec-Rychter M, et al. First evidence of treatment efficacy in metastatic carcinoma of the parotid gland with BRD4/NUT translocation. J Chemother. 2016;28(3):242–6.CrossRef
12.
go back to reference Andreasen S, French CA, Josiassen M, et al. NUT carcinoma of the sublingual gland. Head Neck Pathol. 2016;10(3):362–6.CrossRef Andreasen S, French CA, Josiassen M, et al. NUT carcinoma of the sublingual gland. Head Neck Pathol. 2016;10(3):362–6.CrossRef
13.
go back to reference Seim NB, Philips RHW, Schoenfield L, et al. NUT midline carcinoma of the sublingual gland: clinical presentation and review. Head Neck Pathol. 2017;11(4):460–8.CrossRef Seim NB, Philips RHW, Schoenfield L, et al. NUT midline carcinoma of the sublingual gland: clinical presentation and review. Head Neck Pathol. 2017;11(4):460–8.CrossRef
14.
go back to reference Agaimy A, Fonseca I, Martins C, et al. NUT carcinoma of the salivary glands: clinicopathologic and molecular analysis of 3 cases and a survey of NUT expression in salivary gland carcinomas. Am J Surg Pathol. 2018;42(7):877–84.CrossRef Agaimy A, Fonseca I, Martins C, et al. NUT carcinoma of the salivary glands: clinicopathologic and molecular analysis of 3 cases and a survey of NUT expression in salivary gland carcinomas. Am J Surg Pathol. 2018;42(7):877–84.CrossRef
15.
go back to reference French CA, Miyoshi I, Kubonishi I, et al. BRD4-NUT fusion oncogene: a novel mechanism in aggressive carcinoma. Cancer Res. 2003;63:304–7.PubMed French CA, Miyoshi I, Kubonishi I, et al. BRD4-NUT fusion oncogene: a novel mechanism in aggressive carcinoma. Cancer Res. 2003;63:304–7.PubMed
16.
go back to reference French CA, Miyoshi I, Aster JC, et al. BRD4 bromodomain gene rearrangement in aggressive carcinoma with translocation t(15;19). Am J Pathol. 2001;159(6):1987–92.CrossRef French CA, Miyoshi I, Aster JC, et al. BRD4 bromodomain gene rearrangement in aggressive carcinoma with translocation t(15;19). Am J Pathol. 2001;159(6):1987–92.CrossRef
17.
go back to reference Engleson J, Soller M, Panagopoulos I, et al. Midline carcinoma with t(15;19) and BRD4-NUT fusion oncogene in a 30-year-old female with response to docetaxel and radiotherapy. BMC Cancer. 2006;6:69.CrossRef Engleson J, Soller M, Panagopoulos I, et al. Midline carcinoma with t(15;19) and BRD4-NUT fusion oncogene in a 30-year-old female with response to docetaxel and radiotherapy. BMC Cancer. 2006;6:69.CrossRef
18.
go back to reference Haack H, Johnson LA, Fry CJ, Crosby K, Polakiewicz RD, Stelow EB, Hong SM, Schwartz BE, Cameron MJ, Rubin MA, Chang MC, et al. Diagnosis of NUT midline carcinoma using a NUT-specific monoclonal antibody. Am J Surg Pathol. 2009;33:984–91.CrossRef Haack H, Johnson LA, Fry CJ, Crosby K, Polakiewicz RD, Stelow EB, Hong SM, Schwartz BE, Cameron MJ, Rubin MA, Chang MC, et al. Diagnosis of NUT midline carcinoma using a NUT-specific monoclonal antibody. Am J Surg Pathol. 2009;33:984–91.CrossRef
19.
go back to reference Schwartz BE, Hofer MD, Lemieux ME, et al. Differentiation of NUT midline carcinoma by epigenomic reprogramming. Cancer Res. 2011;71:2686–96.CrossRef Schwartz BE, Hofer MD, Lemieux ME, et al. Differentiation of NUT midline carcinoma by epigenomic reprogramming. Cancer Res. 2011;71:2686–96.CrossRef
20.
go back to reference Mertens F, Wiebe T, Adlercreutz C, et al. Successful treatment of a child with t(15;19)-positive tumor. Pediatr Blood Cancer. 2007;49:1015–7.CrossRef Mertens F, Wiebe T, Adlercreutz C, et al. Successful treatment of a child with t(15;19)-positive tumor. Pediatr Blood Cancer. 2007;49:1015–7.CrossRef
21.
go back to reference Maher OM, Christensen AM, Yedururi S, et al. Histone deacetylase inhibitor for NUT midline carcinoma. Pediatr Blood Cancer. 2015;62:715–7.CrossRef Maher OM, Christensen AM, Yedururi S, et al. Histone deacetylase inhibitor for NUT midline carcinoma. Pediatr Blood Cancer. 2015;62:715–7.CrossRef
22.
go back to reference French CA, Ramirez CL, Kolmakova J, et al. BRD-NUT oncoproteins: a family of closely related nuclear proteins that block epithelial differentiation and maintain the growth of carcinoma cells. Oncogene. 2008;27:2237–42.CrossRef French CA, Ramirez CL, Kolmakova J, et al. BRD-NUT oncoproteins: a family of closely related nuclear proteins that block epithelial differentiation and maintain the growth of carcinoma cells. Oncogene. 2008;27:2237–42.CrossRef
23.
go back to reference Filippakopoulos P, Qi J, Picaud S, et al. Selective inhibition of BET bromodomains. Nature. 2010;468(7327):1067–73.CrossRef Filippakopoulos P, Qi J, Picaud S, et al. Selective inhibition of BET bromodomains. Nature. 2010;468(7327):1067–73.CrossRef
24.
go back to reference Alekseyenko AA, Walsh EM, Wang X, et al. The oncogenic BRD4-NUT chromatin regulator drives aberrant transcription within large topological domains. Genes Dev. 2015;29(14):1507–23.CrossRef Alekseyenko AA, Walsh EM, Wang X, et al. The oncogenic BRD4-NUT chromatin regulator drives aberrant transcription within large topological domains. Genes Dev. 2015;29(14):1507–23.CrossRef
25.
go back to reference Stathis A, Zucca E, Bekradda M, et al. Clinical response of carcinomas harboring the BRD4-NUT oncoprotein to the targeted bromodomain inhibitor OTX015/MK-8628. Cancer Discov. 2016;6(5):492–500.CrossRef Stathis A, Zucca E, Bekradda M, et al. Clinical response of carcinomas harboring the BRD4-NUT oncoprotein to the targeted bromodomain inhibitor OTX015/MK-8628. Cancer Discov. 2016;6(5):492–500.CrossRef
26.
go back to reference Napolitano M, Venturelli M, Molinaro E, et al. NUT midline carcinoma of the head and neck: current perspectives. Onco Targets Ther. 2019;12:3235–44.CrossRef Napolitano M, Venturelli M, Molinaro E, et al. NUT midline carcinoma of the head and neck: current perspectives. Onco Targets Ther. 2019;12:3235–44.CrossRef
27.
go back to reference Weichert W. HDAC expression and clinical prognosis in human malignancies. Cancer Lett. 2009;280(2):168–76.CrossRef Weichert W. HDAC expression and clinical prognosis in human malignancies. Cancer Lett. 2009;280(2):168–76.CrossRef
28.
go back to reference Manzotti G, Ciarrocchi A, Sancisi V. Inhibition of BET proteins and histone deacetylase (HDACs): crossing roads in cancer therapy. Cancers (Basel). 2019;11(3):304.CrossRef Manzotti G, Ciarrocchi A, Sancisi V. Inhibition of BET proteins and histone deacetylase (HDACs): crossing roads in cancer therapy. Cancers (Basel). 2019;11(3):304.CrossRef
29.
go back to reference Zhang H, Shang YP, Chen HY, et al. Histone deacetylases function as novel potential therapeutic target for cancer. Hepatol Res. 2017;47(2):149–59.CrossRef Zhang H, Shang YP, Chen HY, et al. Histone deacetylases function as novel potential therapeutic target for cancer. Hepatol Res. 2017;47(2):149–59.CrossRef
30.
go back to reference Niegish G, Knievel J, Koch A, et al. Changes in histone deacetylase (HDAC) expression patterns and activity of HDAC inhibitors in urothelial cancers. Urol Oncol. 2013;31(8):1770–9.CrossRef Niegish G, Knievel J, Koch A, et al. Changes in histone deacetylase (HDAC) expression patterns and activity of HDAC inhibitors in urothelial cancers. Urol Oncol. 2013;31(8):1770–9.CrossRef
31.
go back to reference Sakuma T, Uzawa K, Onda T, et al. Aberrant expression of histone deacetylase 6 in oral squamous cell carcinoma. Int J Oncol. 2006;29(1):117–24.PubMed Sakuma T, Uzawa K, Onda T, et al. Aberrant expression of histone deacetylase 6 in oral squamous cell carcinoma. Int J Oncol. 2006;29(1):117–24.PubMed
32.
go back to reference Cao J, Lv W, Wang L, et al. Ricolinostat (ACY-1215) suppresses proliferation and promotes apoptosis in esophageal squamous cell carcinoma via miR-30d/PI3K/AKT/mTOR and ERK pathways. Cell Death Dis. 2018;9(8):817.CrossRef Cao J, Lv W, Wang L, et al. Ricolinostat (ACY-1215) suppresses proliferation and promotes apoptosis in esophageal squamous cell carcinoma via miR-30d/PI3K/AKT/mTOR and ERK pathways. Cell Death Dis. 2018;9(8):817.CrossRef
33.
go back to reference Zeng LS, Yang XZ, Wen YF, et al. Overexpressed HDAC4 is associated with poor survival and promotes tumor progression in esophageal carcinoma. Aging (Albany, NY). 2016;8(6):1236–48.CrossRef Zeng LS, Yang XZ, Wen YF, et al. Overexpressed HDAC4 is associated with poor survival and promotes tumor progression in esophageal carcinoma. Aging (Albany, NY). 2016;8(6):1236–48.CrossRef
34.
go back to reference Li S, Wang F, Qu Y, et al. HDAC2 regulates cell proliferation, cell cycle progression and cell apoptosis in esophageal squamous cell carcinoma EC9706 cells. Oncol Lett. 2017;13(1):403–9.CrossRef Li S, Wang F, Qu Y, et al. HDAC2 regulates cell proliferation, cell cycle progression and cell apoptosis in esophageal squamous cell carcinoma EC9706 cells. Oncol Lett. 2017;13(1):403–9.CrossRef
35.
go back to reference Ahn MY. HDAC inhibitor apicidin suppresses murine oral squamous cell carcinoma cell growth in vitro and in vivo via inhibiting HDAC8 expression. Oncol Lett. 2018;16(5):6552–600.PubMedPubMedCentral Ahn MY. HDAC inhibitor apicidin suppresses murine oral squamous cell carcinoma cell growth in vitro and in vivo via inhibiting HDAC8 expression. Oncol Lett. 2018;16(5):6552–600.PubMedPubMedCentral
Metadata
Title
HDAC Overexpression in a NUT Midline Carcinoma of the Parotid Gland with Exceptional Survival: A Case Report
Authors
Gonçalo Esteves
Joana Ferreira
Rita Afonso
Carmo Martins
Carlos Zagalo
Ana Félix
Publication date
01-12-2020
Publisher
Springer US
Published in
Head and Neck Pathology / Issue 4/2020
Electronic ISSN: 1936-0568
DOI
https://doi.org/10.1007/s12105-020-01130-6

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