Literature DB >> 29144820

PHEOCHROMOCYTOMA: A GENETIC AND DIAGNOSTIC UPDATE.

Leilani B Mercado-Asis, Katherine I Wolf, Ivana Jochmanova, David Taïeb.   

Abstract

OBJECTIVE: Pheochromocytomas and paragangliomas (PPGLs) are neuroendocrine tumors derived from adrenal or extra-adrenal locations, respectively. Upon suspicion of PPGL, specific metabolomic, molecular, biochemical, imaging, and histopathologic studies are performed to prove, localize, treat, and monitor disease progression. Improved diagnostic tools allow physicians to accurately diagnose PPGL, even in patients presenting with small (<1 cm) or biochemically silent tumors, which previously delayed proper detection and treatment.
METHODS: This review outlines the most updated approach to PPGL patients and presents a new diagnostic protocol for physicians to increase earlier tumor identification and accurately assess metastatic behavior.
CONCLUSION: We present the most recent advances in genetics, epigenetics, metabolomics, biochemical, and imaging diagnoses of this rare tumor to properly assess disease, decide treatment options, and manage follow-up. We also elaborate on new therapeutic perspectives in these very rare neoplastic entities. ABBREVIATIONS: ATRX = ATRX chromatin remodeler; ccRCC = clear cell renal cell carcinoma; c-MYC = MYC proto oncognene; CT = computed tomography; DOTATATE = DOTA-octreotate; EGLN1/2 = egl-9 family hypoxia inducible factor 1/2; EGLN2/PHD1 = egl-9 family hypoxia inducible factor 2; EPAS1/HIF2A = endothelial PAS domain protein 2/hypoxia-inducible factor 2α; ERK = extracellular signal-regulated kinase; HIFs = hypoxia-inducible factors; HIF-α = hypoxia-inducible factor alpha; HNPGLs = head and neck paragangliomas; 177Lu-DOTATATE = lutetium octreotate; MAX = myc-associated factor X; MDH2 = malate dehydrogenase; MIBG = metaiodobenzylguanidine; MN = metanephrine; MRI = magnetic resonance imaging; mTOR = mammalian target of rapamycin; NETs = neuroendocrine tumors; NF1 = neurofibromin 1; NMN = normetanephrine; PHD = prolyl hydroxylase domain protein; PI3K = phosphoinositide 3-kinase; PPGLs = pheochromocytoma and paragangliomas; PRRT = peptide receptor radionuclide therapy; Pvhl = von Hippel-Lindau protein; RAS = rat sarcoma oncogene; RET = rearranged during transfection proto-oncogene; SDH = succinate dehydrogenase; SDHA, -B, -C, -D = succinate dehydrogenase subunits A, B, C, D; SDHAF2 = succinate dehydrogenase complex assembly factor 2; SDHB, C, D = succinate dehydrogenase subunits B, C, D; SDHx = succinate dehydrogenase subunits; SSTRs = somatostatin receptors; VHL = von Hippel-Lindau.

Entities:  

Mesh:

Year:  2017        PMID: 29144820     DOI: 10.4158/EP-2017-0057

Source DB:  PubMed          Journal:  Endocr Pract        ISSN: 1530-891X            Impact factor:   3.443


  9 in total

Review 1.  The crosstalk between bone remodeling and energy metabolism: A translational perspective.

Authors:  Gerard Karsenty; Sundeep Khosla
Journal:  Cell Metab       Date:  2022-05-10       Impact factor: 31.373

Review 2.  The systems of metastatic potential prediction in pheochromocytoma and paraganglioma.

Authors:  Yong Wang; Minghao Li; Hao Deng; Yingxian Pang; Longfei Liu; Xiao Guan
Journal:  Am J Cancer Res       Date:  2020-03-01       Impact factor: 6.166

Review 3.  Pheochromocytoma/paraganglioma: recent updates in genetics, biochemistry, immunohistochemistry, metabolomics, imaging and therapeutic options.

Authors:  Karren Antonio; Ma Margarita Noreen Valdez; Leilani Mercado-Asis; David Taïeb; Karel Pacak
Journal:  Gland Surg       Date:  2020-02

4.  The Role of the Metabolome and Non-Coding RNA on Pheochromocytomas and Paragangliomas: An Update.

Authors:  Bruno Bouça; Paula Bogalho; Manfredi Rizzo; José Silva-Nunes
Journal:  Metabolites       Date:  2022-02-01

5.  Unusual Long Survival with a Giant Invasive Pheochromocytoma of an Incompatible Patient.

Authors:  Asli Nar
Journal:  Cureus       Date:  2018-03-13

6.  Successful Second-Line Metronomic Temozolomide in Metastatic Paraganglioma: Case Reports and Review of the Literature.

Authors:  Isabel Tena; Garima Gupta; Marcos Tajahuerce; Marta Benavent; Manuel Cifrián; Alejandro Falcon; María Fonfria; Maribel Del Olmo; Rosa Reboll; Antonio Conde; Francisca Moreno; Julia Balaguer; Adela Cañete; Rosana Palasí; Pilar Bello; Alfredo Marco; José Luis Ponce; Juan Francisco Merino; Antonio Llombart; Alfredo Sanchez; Karel Pacak
Journal:  Clin Med Insights Oncol       Date:  2018-04-09

7.  Mutation Profile of Aggressive Pheochromocytoma and Paraganglioma with Comparison of TCGA Data.

Authors:  Yun Mi Choi; Jinyeong Lim; Min Ji Jeon; Yu-Mi Lee; Tae-Yon Sung; Eun-Gyoung Hong; Ji-Young Lee; Se Jin Jang; Won Gu Kim; Dong Eun Song; Sung-Min Chun
Journal:  Cancers (Basel)       Date:  2021-05-14       Impact factor: 6.639

8.  Multidisciplinary practice guidelines for the diagnosis, genetic counseling and treatment of pheochromocytomas and paragangliomas.

Authors:  R Garcia-Carbonero; F Matute Teresa; E Mercader-Cidoncha; M Mitjavila-Casanovas; M Robledo; I Tena; C Alvarez-Escola; M Arístegui; M R Bella-Cueto; C Ferrer-Albiach; F A Hanzu
Journal:  Clin Transl Oncol       Date:  2021-05-06       Impact factor: 3.405

9.  Composite pheochromocytoma/paraganglioma-ganglioneuroma: analysis of SDH and ATRX status, and identification of frequent HRAS and BRAF mutations.

Authors:  Jingci Chen; Yan Wu; Pengyan Wang; Huanwen Wu; Anli Tong; Xiaoyan Chang
Journal:  Endocr Connect       Date:  2021-08-11       Impact factor: 3.335

  9 in total

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