Large Intestinal Cancer
Copyright ©The Author(s) 2002. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Aug 15, 2002; 8(4): 674-678
Published online Aug 15, 2002. doi: 10.3748/wjg.v8.i4.674
Transforming growth factor-β1 in invasion and metastasis in colorectal cancer
Bin Xiong, Hong-Yin Yuan, Ming-Bo Hu, Feng Zhang, Zheng-Zhuan Wei, Ling-Ling Gong, Guo-Liang Yang
Bin Xiong, Hong-Yin Yuan, Ming-Bo Hu, Feng Zhang, Zheng-Zhuan Wei, Ling-Ling Gong, Guo-Liang Yang, Department of Oncology, Affiliated Zhongnan Hospital of Wuhan University, Wuhan 430071, Hubei Province, China
Author contributions: All authors contributed equally to the work.
Supported by Hubei Province Natural Science Foundation, No.2000J054
Correspondence to: Dr. Bin Xiong, Department of Oncology, Affiliated Zhongnan Hospital of Wuhan University, Wuhan 430071, Hubei Province, China. xbxh@public.wh.hb.cn
Telephone: +86-27-87325716
Received: August 8, 2001
Revised: September 15, 2001
Accepted: September 20, 2001
Published online: August 15, 2002
Abstract

AIM: To investigate the role of TGFβ1 in invasion and metastasis in colorectal cancer by analysing TGFβ1 correlated with depth of tumor invasion, stage and metastasis.

METHODS: Serum TGFβ1 levels were determined in 50 patients with colorectal cancer and 30 healthy volunteers using a TGFβ1 enzyme-linked immunosorbent assay. TGFβ1 expression in primary and lymph node metastatic lesions were detected in 98 cases of colorectal cancer by immunohistochemical staining and in situ hybridization.

RESULTS: Serum levels of TGFβ1 in patients with colorectal cancer (40 ± 18 μg·L-1) were significantly higher than those in the healthy control group (19 ± 8 μg·L-1), P < 0.05. Elevated levels of serum TGFβ1 were found in 60% of patients with colorectal cancer when the mean +2 s was used as the upper limit of the normal range (35.1 μg·L-1). Increases in serum TGFβ1 levels were significantly associated with Duke's stage (P < 0.05), but there was no significant difference between Duke's stage B patients and Duke's stage C patients. In the cytoplasm of cancer cells, TGFβ1 was immunostained in 37.8% (37/98) of colorectal cancer, and this expression was confirmed by in situ hybridization. Among 35 cases of colorectal cancer with lymph node metastatic lesions, TGFβ1 positive staining was found in 18 (51.4%) cases of primary tumor, and 25 (71.4%) cases with lymph node metastatic lesions, respectively. Of 17 cases w ith no staining in the primary lesion, 7 (41.2%) casesshowed TGFβ1 staining in the metastatic lesion. Serum TGFβ1 levels and TGFβ1 expression in colorectal cancer tissues were correlated significantly with depth of tumor invasion, stage and metastasis. Patients in stage C-D, T3-T4 and with metastasis had significantly higher TGFβ1 levels than patients in stage A-B, T1-T2 and without metastasis (P < 0.05).

CONCLUSION: These results suggest that transforming growth factor-β1 is closely related to the invasion and metastasis of colorectal cancer. It increased the invasive and metastatic potential of tumor by altering a tumor microenvironment. TGFβ1 may be used as a possible biomarker.

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