Inhibition of oestrone sulphatase activity in the MDA-MB-231 breast cancercell line by breast cyst fluid from Malaysian women

Citation
Re. Elsadig et al., Inhibition of oestrone sulphatase activity in the MDA-MB-231 breast cancercell line by breast cyst fluid from Malaysian women, ANTICANC R, 21(4A), 2001, pp. 2693-2696
Citations number
13
Categorie Soggetti
Onconogenesis & Cancer Research
Journal title
ANTICANCER RESEARCH
ISSN journal
02507005 → ACNP
Volume
21
Issue
4A
Year of publication
2001
Pages
2693 - 2696
Database
ISI
SICI code
0250-7005(200107/08)21:4A<2693:IOOSAI>2.0.ZU;2-E
Abstract
oestrone sulphate is a major source of active oestrogens in the breast. It is converted to oestrone by oestrone sulphatase. Breast cyst fluid (BCF) is a rich source of sex hormones and growth factors. BCF obtained from Britis h women has been shown to inhibit oestrone sulphatase activity in the MCF-7 oestrogen-receptor-positive breast cancer cell line. The aim of the presen t study was to assess whether BCF obtained from Malaysian women inhibited o estrone sulphatase activity in the MCF-7 and MDA-MB-231 breast cancer cell lines. The cell lines were grown in supplemented Dulbecco's Modified Eagle Medium for 3 days, following which a 3-day incubation with sterilised BCF w as carried out. At the end of the treatment period the cell monolayers were assayed for oestrone sulphatase activity and the number of cell nuclei cou nted on a Coulter Counter. BCF was also fractionated on a Bio-Sil SEC 125-5 column by HPLC and the effects of the fractions collected on oestrone sulp hatase activity in the MDA-MB-231 cell line were assessed. All 18 samples o f BCF tested inhibited cell growth in the MDA-MB-231 cell line while 8 out of 10 samples inhibited MCF-7 cell growth; 15 out of 18 BCF samples inhibit ed oestrone sulphatase activity in the MDA-MB-231 cell line whereas 5 out o f 10 samples stimulated oestrone sulphatase activity in the MCF-7 cell line . HPLC fractions corresponding to molecular weights of > 158 kDa and 28 kDa were found to inhibit oestrone sulphatase activity in the MDA-MB-231 cell line. Further work is required to fully characterise these substances as th ey may have roles to play in the prevention of breast cancer.