Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2002 Nov;7(5):205-10.
doi: 10.1007/BF02898006.

Effects ofcis-9,trans-11-conjugated linoleic acid on cancer cell cycle

Affiliations

Effects ofcis-9,trans-11-conjugated linoleic acid on cancer cell cycle

Jia Ren Liu et al. Environ Health Prev Med. 2002 Nov.

Abstract

Objectives: To determine the effect of cis-9, trans-11-conjugated linoleic acid on the cell cycle of mammary cancer cells (MCF-7) and its possible mechanism of inhibition cancer growth.

Methods: Using cell culture and immunocytochemical techniques, we examined the cell growth, DNA synthesis, expression of PCNA, cyclin A, B(1), D(1), p16(ink4a) and p21(cip/wafl) of MCF-7 cells which were treated with various c9, t11-CLA concentrations (25 mM, 50 mM, 100 mM and 200 mM) of c9, t11-CLA for 24 and 48 h, with negative controls (0.1% ethanol).

Results: The cell growth and DNA synthesis of MCF-7 cells were inhibited by c9, t11-CLA. MCF-7 cells, after treatment with various c9, t11-CLA doses mentioned above for 8 days, the inhibition frequency was 27.18%, 35.43%, 91.05%, and 92.86%, respectively and the inhibitory effect of c9, t11-CLA on DNA synthesis (except for 25 mM, 24 h) incorporated significantly less(3)H-TdR than did the negative control (P<0.05 andP<0.01). To further investigate the influence on the cell cycle progression, we found that c9, t11-CLA may arrest the cell cycle of MCF-7 cells. Immunocytochemical staining demonstrated that MCF-7 cells preincubated in media supplemented with different c9, t11-CLA concentrations at various times significantly decreased the expressions of PCNA, and Cyclin, A, B(1), D(1) compared with the negative controls (P<0.01), whereas the expressions of p16(ink4a) and p21(cip/wafl), cyclin-dependent kinases inhibitors (CDKI), were increased.

Conclusions: The cell growth and proliferation of MCF-7 cells is inhibited by c9, t11-CLA by blocking the cell cycle, which reduces expressions of cyclin A, B(1), D(1) and enhances expressions of CDKI (p16(ink4a) and p21(cip/wafl)).

Keywords: cell cycle; cis-9; immunocytochemistry; inhibition; mammary adenocarcinoma cells (MCF-7); trans-11-conjugated linoleic acid (c9, t11-CLA).

PubMed Disclaimer

Similar articles

Cited by

References

    1. {'text': '', 'ref_index': 1, 'ids': [{'type': 'PubMed', 'value': '7017215', 'is_inner': True, 'url': 'https://pubmed.ncbi.nlm.nih.gov/7017215/'}]}
    2. Doll R, Peto R. The causes of cancers: quantitative estimates of avoidable risks of cancer in the United States today. J. Natl. Cancer Inst. 1981; 66: 1191–1308. - PubMed
    1. {'text': '', 'ref_index': 1, 'ids': [{'type': 'PubMed', 'value': '321795', 'is_inner': True, 'url': 'https://pubmed.ncbi.nlm.nih.gov/321795/'}]}
    2. Wynder EL, Gorbi GB. Contribution of the environment to cancer incidence: an epidemiological exercise. J. Natl. Cancer Inst. 1977; 58: 825–832. - PubMed
    1. None
    2. Geboers J, Joossens JV, Kesleloot H. Epidemiology of stomach cancer. In: Diet and Human Carcinogenesis. Editors: Joossens JV, Hill MJ, and Geboers J, Elsevier, New York. 1985 p 81–115.
    1. {'text': '', 'ref_index': 1, 'ids': [{'type': 'PubMed', 'value': '3296942', 'is_inner': True, 'url': 'https://pubmed.ncbi.nlm.nih.gov/3296942/'}]}
    2. Hill MJ. Dietary fat and human cancer. Anticancer Res. 1987; 7: 281–292. - PubMed
    1. {'text': '', 'ref_index': 1, 'ids': [{'type': 'PubMed', 'value': '6947105', 'is_inner': True, 'url': 'https://pubmed.ncbi.nlm.nih.gov/6947105/'}]}
    2. Ziegler RG, Morris LE, Blott WJ, Pottern LM, Hoover R, Fraumeni JF. Esophageal cancer among black men in Washington, D.C. J. Natl. Cancer Inst. 1981; 67: 1199–1206. - PubMed