Sino-European Differences in the Genetic Landscape and Clinical Presentation of Pheochromocytoma and Paraganglioma

Author:

Jiang Jingjing12,Zhang Jing12,Pang Yingxian3,Bechmann Nicole4567,Li Minghao35,Monteagudo Maria8,Calsina Bruna8,Gimenez-Roqueplo Anne-Paule910,Nölting Svenja11,Beuschlein Felix1112ORCID,Fassnacht Martin13ORCID,Deutschbein Timo13,Timmers Henri J L M14,Åkerström Tobias15,Crona Joakim16,Quinkler Marcus17ORCID,Fliedner Stephanie M J18,Liu Yujun19,Guo Jianming19,Li Xiaomu12,Guo Wei20,Hou Yingyong21,Wang Cikui3,Zhang Liang3,Xiao Qiao3,Liu Longfei3,Gao Xin12ORCID,Burnichon Nelly910,Robledo Mercedes8,Eisenhofer Graeme45ORCID

Affiliation:

1. Department of Endocrinology and Metabolism, Zhongshan Hospital, Shanghai, China

2. Fudan Institute for Metabolic Diseases, Fudan University, Shanghai, China

3. Department of Urology, Xiangya Hospital, Central South University, Changsha, China

4. Institute of Clinical Chemistry and Laboratory Medicine, Technische Universität Dresden, Germany

5. Department of Medicine III, University Hospital Carl Gustav Carus, Technische Universität Dresden, Germany

6. German Institute of Human Nutrition Potsdam-Rehbruecke, Department of Experimental Diabetology, Nuthetal, Germany

7. German Center for Diabetes Research, München-Neuherberg, Germany

8. Hereditary Endocrine Cancer Group, Spanish National Cancer Research Center and Centro de Investigación Biomédica en Red de Enfermedades Raras, Madrid, Spain

9. Assistance Publique-Hôpitaux de Paris, Hôpital Européen Georges Pompidou, Genetics Department, Paris, France

10. Université de Paris, PARCC, INSERM, Equipe Labellisée par la Ligue contre le Cancer, Paris, France

11. Department of Medicine IV, University Hospital, LMU Munich, Munich, Germany

12. Department of Endocrinology, Diabetology and Clinical Nutrition, Univiersitäts Spital Zürich, Zurich, Switzerland

13. Department of Internal Medicine I, Division of Endocrinology and Diabetes, University Hospital, University of Würzburg, Würzburg, Germany

14. Department of Internal Medicine, Radboud University Medical Center, Nijmegen, The Netherlands

15. Department of Surgical Sciences, Uppsala University, Uppsala, Sweden

16. Department of medical sciences, Uppsala University, Uppsala, Sweden

17. Endocrinology in Charlottenburg, Berlin, Germany

18. First Department of Medicine, University Medical Center Schleswig-Holstein, Lübeck, Germany

19. Department of Urology, Zhongshan Hospital, Fudan University, Shanghai, China

20. Department of Laboratory Medicine, Zhongshan Hospital, Fudan University, Shanghai, China

21. Department of Pathology, Zhongshan Hospital, Fudan University, Shanghai, China

Abstract

Abstract Context Pheochromocytomas and paragangliomas (PPGLs) are characterized by distinct genotype-phenotype relationships according to studies largely restricted to Caucasian populations. Objective To assess for possible differences in genetic landscapes and genotype-phenotype relationships of PPGLs in Chinese versus European populations. Design Cross-sectional study. Setting 2 tertiary-care centers in China and 9 in Europe. Participants Patients with pathologically confirmed diagnosis of PPGL, including 719 Chinese and 919 Europeans. Main Outcome Measures Next-generation sequencing performed in tumor specimens with mutations confirmed by Sanger sequencing and tested in peripheral blood if available. Frequencies of mutations were examined according to tumor location and catecholamine biochemical phenotypes. Results Among all patients, higher frequencies of HRAS, FGFR1, and EPAS1 mutations were observed in Chinese than Europeans, whereas the reverse was observed for NF1, VHL, RET, and SDHx. Among patients with apparently sporadic PPGLs, the most frequently mutated genes in Chinese were HRAS (16.5% [13.6-19.3] vs 9.8% [7.6-12.1]) and FGFR1 (9.8% [7.6-12.1] vs 2.2% [1.1-3.3]), whereas among Europeans the most frequently mutated genes were NF1 (15.9% [13.2-18.6] vs 6.6% [4.7-8.5]) and SDHx (10.7% [8.4–13.0] vs 4.2% [2.6–5.7]). Among Europeans, almost all paragangliomas lacked appreciable production of epinephrine and identified gene mutations were largely restricted to those leading to stabilization of hypoxia inducible factors. In contrast, among Chinese there was a larger proportion of epinephrine-producing paragangliomas, mostly due to HRAS and FGFR1 mutations. Conclusions This study establishes Sino-European differences in the genetic landscape and presentation of PPGLs, including ethnic differences in genotype-phenotype relationships indicating a paradigm shift in our understanding of the biology of these tumors.

Funder

Shanghai Municipal Science and Technology

National Natural Science Foundation of China

Central South University

Deutsche Forschungsgemeinschaft

Instituto de Salud Carlos III

European Regional Development Fund

Paradifference Foundation

Cancer Research for Personalized Medicine

Ligue Nationale contre le Cancer

Institut National du Cancer

Direction Générale de l’Offre de Soins

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference42 articles.

1. Pheochromocytoma and paraganglioma pathogenesis: learning from genetic heterogeneity;Dahia;Nat Rev Cancer.,2014

2. New perspectives on pheochromocytoma and paraganglioma: toward a molecular classification;Crona;Endocr Rev.,2017

3. Genotype-phenotype correlations in pheochromocytoma and paraganglioma: a systematic review and individual patient meta-analysis;Crona;Endocr Relat Cancer.,2019

4. Pheochromocytoma and paraganglioma: genotype versus anatomic location as determinants of tumor phenotype;Fliedner;Cell Tissue Res.,2018

5. Metabologenomics of phaeochromocytoma and paraganglioma: an integrated approach for personalised biochemical and genetic testing;Eisenhofer;Clin Biochem Rev.,2017

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