Literature DB >> 22634690

Expression of androgen, estrogen, progesterone, and growth hormone receptors in vascular malformations.

Ann M Kulungowski1, Aladdin H Hassanein, Vânia Nosé, Steven J Fishman, John B Mulliken, Joseph Upton, David Zurakowski, Amy D DiVasta, Arin K Greene.   

Abstract

BACKGROUND: Vascular malformations frequently enlarge during adolescence, suggesting that hormones may be involved. The purpose of this study was to determine whether pubertal hormone receptors are present in vascular malformations and whether they differ from normal tissue.
METHODS: Tissue specimens (arteriovenous malformation, lymphatic malformation, and venous malformation) were prospectively collected from patients undergoing resection. Immunohistochemistry was used to determine the presence of androgen, estrogen, progesterone, and growth hormone receptors. The effects of age, sex, location, and malformation type on receptor expression were analyzed. Age-, sex-, and location-matched normal tissues served as controls.
RESULTS: Forty-five vascular malformation specimens were collected: arteriovenous malformation (n = 11), lymphatic malformation (n = 20), and venous malformation (n = 14). Growth hormone receptor expression was increased in arteriovenous malformation (72.7 percent), lymphatic malformation (65.0 percent), and venous malformation (57.1 percent) tissues compared with controls (25.8 percent) (p < 0.05). Growth hormone receptor was present primarily in the endothelium/perivasculature of malformations (93.1 percent), whereas in normal tissue growth hormone receptor was located only in the stroma (p < 0.0001). Neither age, nor sex, nor location influenced receptor expression (p = 0.9). No differences in androgen receptor, estrogen receptor, and progesterone receptor staining were found between malformations and control samples (p = 0.7).
CONCLUSIONS: Growth hormone receptor is overexpressed and principally located in the vessels of vascular malformations. Growth hormone might contribute to the expansion of vascular malformations.

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Year:  2012        PMID: 22634690     DOI: 10.1097/PRS.0b013e31824ec3fb

Source DB:  PubMed          Journal:  Plast Reconstr Surg        ISSN: 0032-1052            Impact factor:   4.730


  8 in total

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Authors:  V Salpietro; M Ruggieri; T Alterio; R Mallamace; V Chirico; T Arrigo; C Romano
Journal:  J Endocrinol Invest       Date:  2013-05-22       Impact factor: 4.256

2.  Expansion of pulmonary arteriovenous malformations after grand mal seizures and other circumstances of PAVM growth.

Authors:  Ami Schattner; Ina Dubin
Journal:  BMJ Case Rep       Date:  2019-08-10

3.  Pingyangmycin Pretreatment Influences the Biological Behavior of Ocular Venous Malformation and Relates with Galectin-3 Expression.

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Journal:  Chin Med J (Engl)       Date:  2017-08-05       Impact factor: 2.628

Review 4.  The Endothelium in Acromegaly.

Authors:  Pietro Maffei; Francesca Dassie; Alexandra Wennberg; Matteo Parolin; Roberto Vettor
Journal:  Front Endocrinol (Lausanne)       Date:  2019-07-24       Impact factor: 5.555

Review 5.  Immunomodulation of carcinogens-induced steroids-dependent human diseases.

Authors:  Andrew N Glushkov; Elena G Polenok
Journal:  Saudi J Biol Sci       Date:  2017-10-03       Impact factor: 4.219

Review 6.  A literature review of microvascular proliferation in arteriovenous malformations of skin and soft tissue.

Authors:  Amalia Mulia Utami; Siham Azahaf; Onno J de Boer; Chantal M A M van der Horst; Lorine B Meijer-Jorna; Allard C van der Wal
Journal:  J Clin Transl Res       Date:  2021-07-30

7.  Expression of the Components of the Renin-Angiotensin System in Venous Malformation.

Authors:  Sam Siljee; Emily Keane; Reginald Marsh; Helen D Brasch; Swee T Tan; Tinte Itinteang
Journal:  Front Surg       Date:  2016-05-03

8.  Treatment of Acquired Digital Arteriovenous Malformation with Progression during Pregnancy.

Authors:  Hiroshi Fujimaki; Masaki Takeuchi
Journal:  Plast Reconstr Surg Glob Open       Date:  2019-12-12
  8 in total

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