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Modulation of aromatase activity by growth factors in an androgen sensitive human prostate cancer cell line, LNCaP

*Corresponding author for this work
  • University of Miami
    ,
  • Department of Veterans Affairs
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

The effects of steroids and peptide growth factors on aromatase activity in an androgen sensitive human prostate cancer cell line (LNCaP) were investigated. Factors were selected based on their observed modulation of the enzyme in other tissues. Incubation with epidermal growth factor and transforming growth factor-1 decreased aromatase activity in LNCaP cells by 25-40%. Insulin like growth factor-1, dexamethasone, dibutyryl cAMP and phorbol 12-myristate 13-acetate, all of which are modulators of aromatase in other tissues, had no significant effect on aromatase activity in LNCaP cells. In addition, the cAMP-dependent protein kinase and protein kinase C inhibitor 1-(5-isoquinolinylsulfonyl)-2 methylpiperazine (H-7) had no effect on the enzyme activity. Factors affecting prostatic aromatase may be distinct from those for other known species.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 167-172 (6 pages)

Journal (Volume, Issue Number)

Cancer Letters (Volume 102, Issue 1-2)

Publication milestones

  • Published - 04/19/1996

Publication status

Published - 04/19/1996

ISSN

0304-3835

Publication IDs

  • Scopus: 0029967872
  • PubMed: 8603365

Publication metrics

Metrics

Fractional count
1
Fractional count
0.33
Fractional count
2
Fractional count
0.67
Fractional count
1
Fractional count
1
SciVal
FWCI
0.25
SciVal
Author count
3
SciVal
citations
5
SciVal
Paper percentile
49
Scopus
citations

PlumX, opens in new tab

Captures
6
Citation count
6

Funding Details

The authors thank Marie Selzer. This study was supported in part by an Alpha Omega Alpha Student Research Fellowship to J.L. Block. This work was supported in parts by Wendy Will Cancer Research Award (BLL), NIH Grant No. lR29CA63108 (BLL) and L. Austin Weeks Family Endowment (BLL, NLB).