Research
 • Research Divisions
 • Research Progress
 • Supporting System
 • Achievements
 • Research Programs
 • Technology Transfer
    Home > Research > Research Progress

Raspberry pulp polysaccharides inhibit tumor growth via immunopotentiation and enhance docetaxel chemotherapy against malignant melanoma in vivo

Author: Update time: 01-21-2016 Printer Text Size: A A A

It has been reported previously that the systemic efficacy of chemotherapeutic agents is substantially restricted for some cancer types, including malignant melanoma. Therefore, the development of more effective treatment modalities remains a critical, albeit elusive, goal in anticancer therapy.

The study presented here evaluates the antitumor activity of raspberry pulp polysaccharides (RPPs) against malignant melanoma using a murine tumor-bearing model. Furthermore, the underlying mechanism of this antitumor activity has also been investigated.

The results show that while RPP exhibits no direct cytotoxic effect on HT-29, MGC-803, HeLa, Bel-7402, L02 and B16F10 cells in vitro, it does demonstrate a dose-dependent growth inhibition of melanoma in vivo with an inhibition ratio of 59.95% at a dose of 400 mg kg−1. Besides this, the body weight and spleen index in tumor-bearing mice have also been improved in RPPtreated groups. RPP is also found to induce splenocyte proliferation and is able to upregulate the activity of immune-related enzymes, including acid phosphatase (ACP), alkaline phosphatase (AKP), lactate dehydrogenase (LDH) and superoxide dismutase (SOD) in the spleen of tumor-bearing mice. The levels of tumor necrosis factor α (TNF-α), interferon γ (IFN-γ) and interleukin 2 (IL-2) in the serum of tumorbearing mice show to be effectively increased upon RPP treatment. Histopathological analyses show that RPP induces tumor tissue necrosis by increasing inflammatory cell infiltration and causes no lesions to liver and kidney tissues. Remarkably, RPP further enhances the antitumor effect of the chemotherapeutic drug docetaxel and alleviates docetaxel-induced liver and kidney lesions in tumor-bearing mice. These findings indicate that RPP exhibits antitumor activity in vivo against malignant melanoma, partly by enhancing the cellular immune response of the host organism. In summary, RPP features critical properties to potentially find use as an immunopotentiating agent or as a chemotherapy adjuvant agent for the treatment of malignant melanoma. 


Fig. RPP alleviates liver (A) and kidney (B) injuries induced by docetaxel (H&E stain ×100). ME: mesangial expansion; ICI: inflammatory cell infiltration.

 

Additional Information:

1 Author Information: YANG Yongjing, XU Hanmei, SUO Yourui.
Correspondence: yrsuo@nwipb.cas.cn.
2 Published: Food Funct., 6:3022–3034,2015.

  Attachment:
  CLOSE
TOP TEN
Northwest Institute of Plateau Biology, CAS
Add: 23# Xinning Lu, Xining, Qinghai, China 810008
Tel: +86-971-6143530 Fax: +86-971-6143282