Dark-colored maple syrup treatment induces S-phase cell cycle arrest via reduced proliferating cell nuclear antigen expression in colorectal cancer cells

被引:6
作者
Yamamoto, Tetsushi [1 ]
Nishita, Tomoyo [1 ]
Taga, Atsushi [1 ]
机构
[1] Kindai Univ, Sch Pharm, Pathol & Biomol Anal Lab, 3-4-1 Kowakae, Higashiosaka, Osaka 5778502, Japan
关键词
maple syrup; colorectal cancer; proteomics; cell cycle; proliferating cell nuclear antigen; TOKUSHIMA FATTY RATS; BREAST-CANCER; DAIRY-PRODUCTS; PLASMA-GLUCOSE; RISK; FOODS; PCNA; CALCIUM; SAP; IDENTIFICATION;
D O I
10.3892/ol.2019.9928
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Maple syrup is a natural sweetener that is consumed worldwide. It has been previously reported that dark-colored maple syrup exerts an inhibitory effect on colorectal cancer (CRC) proliferation and invasion. In the present study, the underlying mechanism of CRC cell growth inhibition was examined with dark-colored maple syrup treatment using a shotgun liquid chromatography-tandem mass spectrometry-based global proteomic approach. Applying a semi-quantitative method based on spectral counting, 388 proteins were identified with expression changes of >1.5-fold following dark-colored maple syrup treatment. Gene Ontology analysis revealed that these proteins possessed cell cycle-associated functions. It was also indicated that CRC cells treated with dark-colored maple syrup exhibited decreased proliferating cell nuclear antigen (PCNA) expression and S-phase cell cycle arrest. Dark-colored maple syrup treatment also resulted in altered expression of cell cycle-associated genes, including cyclin-dependent kinase (CDK)4 and CDK6. In conclusion, these data suggested that dark-colored maple syrup induced S-phase cell cycle arrest in CRC cells by reducing the expression of PCNA and regulating cell cycle-associated genes. These findings suggest that dark-colored maple syrup may be a source of compounds for the development of novel drugs for colorectal cancer treatment.
引用
收藏
页码:2713 / 2720
页数:8
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共 58 条
  • [1] Analysis of rpoS and bolA gene expression under various stress-induced environments in planktonic and biofilm phase using 2-ΔΔCT method
    Adnan, Mohd
    Morton, Glyn
    Hadi, Sibte
    [J]. MOLECULAR AND CELLULAR BIOCHEMISTRY, 2011, 357 (1-2) : 275 - 282
  • [2] In vitro evaluation of phenolic-enriched maple syrup extracts for inhibition of carbohydrate hydrolyzing enzymes relevant to type 2 diabetes management
    Apostolidis, Emmanouil
    Li, Liya
    Lee, Chong
    Seeram, Navindra P.
    [J]. JOURNAL OF FUNCTIONAL FOODS, 2011, 3 (02) : 100 - 106
  • [3] ENVIRONMENTAL FACTORS AND CANCER INCIDENCE AND MORTALITY IN DIFFERENT COUNTRIES, WITH SPECIAL REFERENCE TO DIETARY PRACTICES
    ARMSTRONG, B
    DOLL, R
    [J]. INTERNATIONAL JOURNAL OF CANCER, 1975, 15 (04) : 617 - 631
  • [4] USE OF PLANTS FOR FOOD AND MEDICINE BY NATIVE PEOPLES OF EASTERN CANADA
    ARNASON, T
    HEBDA, RJ
    JOHNS, T
    [J]. CANADIAN JOURNAL OF BOTANY-REVUE CANADIENNE DE BOTANIQUE, 1981, 59 (11): : 2189 - 2325
  • [5] The chemical composition of maple syrup
    Ball, David W.
    [J]. JOURNAL OF CHEMICAL EDUCATION, 2007, 84 (10) : 1647 - U6
  • [6] PCNA is recruited to irradiated chromatin in late S-phase and is most pronounced in G2 phase of the cell cycle
    Bartova, Eva
    Suchankova, Jana
    Legartova, Sona
    Malyskova, Barbora
    Hornacek, Matus
    Skalnikova, Magdalena
    Masata, Martin
    Raska, Ivan
    Kozubek, Stanislav
    [J]. PROTOPLASMA, 2017, 254 (05) : 2035 - 2043
  • [7] Monitoring protein expression in whole-cell extracts by targeted label- and standard-free LC-MS/MS
    Bluemlein, Katharina
    Ralser, Markus
    [J]. NATURE PROTOCOLS, 2011, 6 (06) : 859 - 869
  • [8] How is epigenetic information maintained through DNA replication?
    Budhavarapu, Varija N.
    Chavez, Myrriah
    Tyler, Jessica K.
    [J]. EPIGENETICS & CHROMATIN, 2013, 6
  • [9] IL-27 mediates HLA class I up-regulation, which can be inhibited by the IL-6 pathway, in HLA-deficient Small Cell Lung Cancer cells
    Carbotti, Grazia
    Nikpoor, Amin Reza
    Vacca, Paola
    Gangemi, Rosaria
    Giordano, Chiara
    Campelli, Francesco
    Ferrini, Silvano
    Fabbi, Marina
    [J]. JOURNAL OF EXPERIMENTAL & CLINICAL CANCER RESEARCH, 2017, 36