Literature DB >> 9591212

Serum levels of dimeric activin A are not a marker of placental tumors in the course of chemotherapy.

P Florio1, S Luisi, E Casarosa, A R Genazzani, P Pautier, C Lhommé, J M Bidart, P G Driul, F Petraglia.   

Abstract

The aim of the present study was to evaluate whether serum activin A levels may represent, in addition to intact human chorionic gonadotrophin, a marker of placental tumors in the course of chemotherapy. Serial determinations of serum levels of activin A were performed in women with hydatidiform mole (n = 2) or choriocarcinoma (n = 3). Serum activin A levels were measured by using a new specific two-site enzyme immunoassay (EIA) able to detect the dimeric, bioactive, form of the protein. Serum hCG concentrations in samples taken after evacuation before starting chemotherapy were greater than in healthy non-pregnant women (p < 0.001) and decreased following chemotherapy. Activin A serum levels in women with trophoblastic disease after evacuation were significantly higher than in healthy non-pregnant women, but chemotherapy did not significantly affect circulating levels. No correlation was found between changes of activin A and total hCG serum concentrations. Measurement of activin A by ELISA in presence of persistent molar tumor does not seem to be of clinical interest in the follow-up of disease, resulting activin A concentrations after chemotherapy in the range of values occurring throughout menstrual cycle. These evidences suggest that hCG determination is still the most valid for follow-up, because only intact hCG could detect the persistence of trophoblast tissue.

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Year:  1998        PMID: 9591212     DOI: 10.1007/BF03347296

Source DB:  PubMed          Journal:  J Endocrinol Invest        ISSN: 0391-4097            Impact factor:   4.256


  10 in total

Review 1.  Peptide signaling in human placenta and membranes: autocrine, paracrine, and endocrine mechanisms.

Authors:  F Petraglia; P Florio; C Nappi; A R Genazzani
Journal:  Endocr Rev       Date:  1996-04       Impact factor: 19.871

Review 2.  Inhibins and activins: roles in clinical practice.

Authors:  E M Wallace; D L Healy
Journal:  Br J Obstet Gynaecol       Date:  1996-10

3.  High concentrations of plasma immunoreactive inhibin during normal pregnancy in women.

Authors:  Y Abe; Y Hasegawa; K Miyamoto; M Yamaguchi; A Andoh; Y Ibuki; M Igarashi
Journal:  J Clin Endocrinol Metab       Date:  1990-07       Impact factor: 5.958

4.  Immunohistochemical localization of inhibin-activin subunits in hydatidiform mole and invasive mole.

Authors:  S Minami; M Yamoto; R Nakano
Journal:  Obstet Gynecol       Date:  1993-09       Impact factor: 7.661

5.  Changes in peripheral serum levels of total activin A during the human menstrual cycle and pregnancy.

Authors:  S Muttukrishna; P A Fowler; L George; N P Groome; P G Knight
Journal:  J Clin Endocrinol Metab       Date:  1996-09       Impact factor: 5.958

6.  Inhibin: a new circulating marker of hydatidiform mole?

Authors:  T Yohkaichiya; T Fukaya; H Hoshiai; A Yajima; D M de Kretser
Journal:  BMJ       Date:  1989-06-24

7.  Hypertension in pregnancy: changes in activin A maternal serum concentration.

Authors:  F Petraglia; L Aguzzoli; A Gallinelli; P Florio; M Zonca; C Benedetto; K Woodruff
Journal:  Placenta       Date:  1995-07       Impact factor: 3.481

8.  Activin at parturition: changes of maternal serum levels and evidence for binding sites in placenta and fetal membranes.

Authors:  F Petraglia; A Gallinelli; D De Vita; K Lewis; L Mathews; W Vale
Journal:  Obstet Gynecol       Date:  1994-08       Impact factor: 7.661

9.  Abnormal concentration of maternal serum activin-A in gestational diseases.

Authors:  F Petraglia; D De Vita; A Gallinelli; L Aguzzoli; A R Genazzani; R Romero; T K Woodruff
Journal:  J Clin Endocrinol Metab       Date:  1995-02       Impact factor: 5.958

10.  Inhibin as a marker for hydatidiform mole: a comparative study with the determinations of intact human chorionic gonadotrophin and its free beta-subunit.

Authors:  Y Badonnel; F Barbé; H Legagneur; E Poncelet; M Schweitzer
Journal:  Clin Endocrinol (Oxf)       Date:  1994-08       Impact factor: 3.478

  10 in total

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