The Correlation between Lipid Metabolism Disorders and Prostate Cancer

被引:13
作者
Dlubek, Justyna [1 ]
Rysz, Jacek [1 ]
Jablonowski, Zbigniew [2 ]
Gluba-Brzozka, Anna [1 ]
Franczyk, Beata [1 ]
机构
[1] Med Univ Lodz, Dept Nephrol Hypertens & Family Med, Zeromskiego 113, PL-90549 Lodz, Poland
[2] Med Univ Lodz, Dept Urol, Zeromskiego 113, PL-90549 Lodz, Poland
关键词
Prostate cancer; carcinogenesis; cholesterol levels; lipids disorders; metastasis; cells growth; gene therapy; FATTY-ACID SYNTHASE; PCSK9 REGULATES APOPTOSIS; DE-NOVO LIPOGENESIS; SERUM-CHOLESTEROL; CELLS; RISK; EXPRESSION; BREAST; GENE; PROGRESSION;
D O I
10.2174/0929867327666200806103744
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Prostate cancer is the second most common cancer affecting the male population all over the world. The existence of a correlation between lipid metabolism disorders and cancer of the prostate gland has been widely known for a long time. According to hypotheses, cholesterol may contribute to prostate cancer progression as a result of its participation as a signaling molecule in prostate growth and differentiation via numerous biologic mechanisms including Akt signaling and de novo steroidogenesis. The results of some studies suggest that increased cholesterol levels may be associated with a higher risk of a more aggressive course of the disease. The aforementioned alterations in the synthesis of fatty acids are a unique feature of cancer and, therefore, constitute an attractive target for therapeutic intervention in the treatment of prostate cancer. Pharmacological or gene therapy aims to reduce the activity of enzymes involved in de novo synthesis of fatty acids, FASN, ACLY (ATP citrate lyase) or SCD-1 (Stearoyl- CoA Desaturase) in particular, that may result in cells growth arrest. Nevertheless, not all cancers are unequivocally associated with hypocholesterolaemia. It cannot be ruled out that the relationship between prostate cancer and lipid disorders is not a direct quantitative correlation between carcinogenesis and the amount of circulating cholesterol. Perhaps the correspondence is more sophisticated and connected to the distribution of cholesterol fractions or even sub-fractions of e.g. HDL cholesterol.
引用
收藏
页码:2048 / 2061
页数:14
相关论文
共 109 条
  • [1] Diagnostic value of lipids, total antioxidants, and trace metals in benign prostate hyperplasia and prostate cancer
    Adedapo, K. S.
    Arinola, O. G.
    Shittu, O. B.
    Kareem, O. I.
    Okolo, C. A.
    Nwobi, L. N.
    [J]. NIGERIAN JOURNAL OF CLINICAL PRACTICE, 2012, 15 (03) : 293 - 297
  • [2] Serum Lipid Profile and Risk of Prostate Cancer Recurrence: Results from the SEARCH Database
    Allott, Emma H.
    Howard, Lauren E.
    Cooperberg, Matthew R.
    Kane, Christopher J.
    Aronson, William J.
    Terris, Martha K.
    Amling, Christopher L.
    Freedland, Stephen J.
    [J]. CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION, 2014, 23 (11) : 2349 - 2356
  • [3] Alo PL, 1996, CANCER, V77, P474, DOI 10.1002/(SICI)1097-0142(19960201)77:3<474::AID-CNCR8>3.0.CO
  • [4] 2-K
  • [5] Serum lipids as markers of prostate cancer occurrence and prognosis?
    Arthur, Rhonda
    Rodriguez-Vida, Alejo
    Zadra, Giorgia
    Moller, Henrik
    Van Hemelrijck, Mieke
    [J]. CLINICAL LIPIDOLOGY, 2015, 10 (02) : 145 - 165
  • [6] The role of choline in prostate cancer
    Awwad, Hussain Mohamad
    Geisel, Juergen
    Obeid, Rima
    [J]. CLINICAL BIOCHEMISTRY, 2012, 45 (18) : 1548 - 1553
  • [7] International epidemiology of prostate cancer: Geographical distribution and secular trends
    Baade, Peter D.
    Youlden, Danny R.
    Krnjacki, Lauren J.
    [J]. MOLECULAR NUTRITION & FOOD RESEARCH, 2009, 53 (02) : 171 - 184
  • [8] Androgen-regulated metabolism and biosynthesis in prostate cancer
    Barfeld, Stefan J.
    Itkonen, Harri M.
    Urbanucci, Alfonso
    Mills, Ian G.
    [J]. ENDOCRINE-RELATED CANCER, 2014, 21 (04) : T57 - T66
  • [9] Chemical inhibition of Acetyl-CoA carboxylase induces growth arrest and cytotoxicity selectively in cancer cells
    Beckers, Annelies
    Organe, Sophie
    Tinunermans, Leen
    Scheys, Katryn
    Peeters, Annelies
    Brusselmans, Koen
    Verhoeven, Guido
    Swinnen, Johannes V.
    [J]. CANCER RESEARCH, 2007, 67 (17) : 8180 - 8187
  • [10] Changes in Gene Transcription Underlying the Aberrant Citrate and Choline Metabolism in Human Prostate Cancer Samples
    Bertilsson, Helena
    Tessem, May-Britt
    Flatberg, Amar
    Viset, Trond
    Gribbestad, Ingrid
    Angelsen, Anders
    Halgunset, Jostein
    [J]. CLINICAL CANCER RESEARCH, 2012, 18 (12) : 3261 - 3269