Chitosan oligosaccharides with degree of polymerization 2–6 induces apoptosis in human colon carcinoma HCT116 cells. (5th January 2018)
- Record Type:
- Journal Article
- Title:
- Chitosan oligosaccharides with degree of polymerization 2–6 induces apoptosis in human colon carcinoma HCT116 cells. (5th January 2018)
- Main Title:
- Chitosan oligosaccharides with degree of polymerization 2–6 induces apoptosis in human colon carcinoma HCT116 cells
- Authors:
- Zou, Pan
Yuan, Shoujun
Yang, Xin
Zhai, Xingchen
Wang, Jing - Abstract:
- Abstract: Colon cancer is the third most common cancer, and yet there is a lack of effective therapeutic method with low side effects. Chitosan oligosaccharides (COS) is derived from chitosan after chitin deacetylation, and attracts more interests due to smaller molecular weight and soluble property. Previously, COS, mainly absorbed through intestinal epithelia, has been reported to exhibit many bioactivities, especially its anti-tumor effect. Recent references pay little attention to molecular weight distribution which is crucial for understanding its biological behavior. Here, we studied reducing sugar content and degree of polymerization (DP) of COS. 86.73% reducing sugar exists in COS sample and the content of chitosan fractions with 2–6 is 85.8%. COS suppressed the growth of HCT116 cells in vitro and in vivo, and the inhibition rate of tumor weight in vivo was high up to 58.6%. Moreover, the morphology observation, flow cytometry analysis and mRNA expression were applied to study the apoptosis related mechanism. COS treatment promoted mitosis, late stage apoptosis and S cell cycle arrest in HCT116 cells, and enhanced the mRNA expression of BAK and reduce BCL-2 and BCL-xL . These findings may provide an important clue for clinical applications of COS as anti-tumor drug or pharmaceutic adjuvant in the future. Graphical abstract: Highlights: The paper highlights the reducing sugar content and degree of polymerization of COS. COS exhibits excellent antitumor effect on humanAbstract: Colon cancer is the third most common cancer, and yet there is a lack of effective therapeutic method with low side effects. Chitosan oligosaccharides (COS) is derived from chitosan after chitin deacetylation, and attracts more interests due to smaller molecular weight and soluble property. Previously, COS, mainly absorbed through intestinal epithelia, has been reported to exhibit many bioactivities, especially its anti-tumor effect. Recent references pay little attention to molecular weight distribution which is crucial for understanding its biological behavior. Here, we studied reducing sugar content and degree of polymerization (DP) of COS. 86.73% reducing sugar exists in COS sample and the content of chitosan fractions with 2–6 is 85.8%. COS suppressed the growth of HCT116 cells in vitro and in vivo, and the inhibition rate of tumor weight in vivo was high up to 58.6%. Moreover, the morphology observation, flow cytometry analysis and mRNA expression were applied to study the apoptosis related mechanism. COS treatment promoted mitosis, late stage apoptosis and S cell cycle arrest in HCT116 cells, and enhanced the mRNA expression of BAK and reduce BCL-2 and BCL-xL . These findings may provide an important clue for clinical applications of COS as anti-tumor drug or pharmaceutic adjuvant in the future. Graphical abstract: Highlights: The paper highlights the reducing sugar content and degree of polymerization of COS. COS exhibits excellent antitumor effect on human colon cancer HCT116 cells. COS induces apoptosis in HCT116 cells. … (more)
- Is Part Of:
- Chemico-biological interactions. Volume 279(2018)
- Journal:
- Chemico-biological interactions
- Issue:
- Volume 279(2018)
- Issue Display:
- Volume 279, Issue 2018 (2018)
- Year:
- 2018
- Volume:
- 279
- Issue:
- 2018
- Issue Sort Value:
- 2018-0279-2018-0000
- Page Start:
- 129
- Page End:
- 135
- Publication Date:
- 2018-01-05
- Subjects:
- Chitosan oligosaccharides -- Degree of polymerization -- Colon cancer -- HCT116 -- Apoptosis
Biochemistry -- Periodicals
Toxicological chemistry -- Periodicals
Biochemistry -- Periodicals
Biologie moléculaire -- Périodiques
Biochimie -- Périodiques
Toxicologie biochimique -- Périodiques
572 - Journal URLs:
- http://www.sciencedirect.com/science/journal/00092797 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.cbi.2017.11.010 ↗
- Languages:
- English
- ISSNs:
- 0009-2797
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3155.500000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 5499.xml