Published January 6, 2012 | Version v1
Journal article

Frizzled-8 as a putative therapeutic target in human lung cancer

  • 1. Department of Medical Oncology, Tianjin Medical University Cancer Hospital, Tianjin 300060 (China)
  • 2. Department of Radiation and Medical Oncology, Zhongnan Hospital, Hubei Cancer Clinical Study Center, Wuhan University, Wuhan 430071 (China)
  • 3. Department of Pathology, Tianjin Chest Hospital, Tianjin 300051 (China)
  • 4. Department of Pathology, Henan Cancer Hospital, Zhengzhou (China)
  • 5. Department of Thoracic Surgery, Xuanwu Hospital, Capital Medical University, Beijing 100053 (China)

Description

Highlights: ► Fzd-8 is over-expressed in human lung cancer. ► shRNA knock-down of Fzd-8 inhibits proliferation and Wnt pathway in lung cancer cells. ► shRNA knock-down of Fzd-8 suppresses tumor growth in vivo. ► shRNA knock-down Fzd-8 sensitizes lung cancer cells to chemotherapy Taxotere. -- Abstract: Lung cancer is the leading cause of cancer related deaths worldwide. It is necessary to better understand the molecular mechanisms involved in lung cancer in order to develop more effective therapeutics for the treatment of this disease. Recent reports have shown that Wnt signaling pathway is important in a number of cancer types including lung cancer. However, the role of Frizzled-8 (Fzd-8), one of the Frizzled family of receptors for the Wnt ligands, in lung cancer still remains to be elucidated. Here in this study we showed that Fzd-8 was over-expressed in human lung cancer tissue samples and cell lines. To investigate the functional importance of the Fzd-8 over-expression in lung cancer, we used shRNA to knock down Fzd-8 mRNA in lung cancer cells expressing the gene. We observed that Fzd-8 shRNA inhibited cell proliferation along with decreased activity of Wnt pathway in vitro, and also significantly suppressed A549 xenograft model in vivo (p < 0.05). Furthermore, we found that knocking down Fzd-8 by shRNA sensitized the lung cancer cells to chemotherapy Taxotere. These data suggest that Fzd-8 is a putative therapeutic target for human lung cancer and over-expression of Fzd-8 may be important for aberrant Wnt activation in lung cancer.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.bbrc.2011.11.055

Additional details

Identifiers

DOI
10.1016/j.bbrc.2011.11.055;
PII
S0006-291X(11)02069-9;

Publishing Information

Journal Title
Biochemical and Biophysical Research Communications
Journal Volume
417
Journal Issue
1
Journal Page Range
p. 62-66
ISSN
0006-291X
CODEN
BBRCA9

INIS

Country of Publication
United States
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
45028530
Subject category
S60: APPLIED LIFE SCIENCES;
Descriptors DEI
ANIMAL TISSUES; CELL PROLIFERATION; CHEMOTHERAPY; DEATH; GENES; IN VITRO; IN VIVO; INHIBITION; LIGANDS; LUNGS; MESSENGER-RNA; NEOPLASMS; RECEPTORS
Descriptors DEC
BODY; DISEASES; MEDICINE; MEMBRANE PROTEINS; NUCLEIC ACIDS; ORGANIC COMPOUNDS; ORGANS; PROTEINS; RESPIRATORY SYSTEM; RNA; THERAPY

Optional Information

Copyright
Copyright (c) 2011 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.