The Role of Lymphangiogenesis in Head and Neck Cancer Metastasis

March 29, 2006 updated by: National Taiwan University Hospital
The purpose of this study is to investigate the role of lymphangiogenesis in the metastasis of head and neck cancer.

Study Overview

Status

Unknown

Conditions

Detailed Description

Head and neck cancer is a major, worldwide cause of morbidity and mortality. As long as the neoplasm is confined to its organ of origin, the patient can be cured through surgical removal of the tumor mass. Unfortunately, many cancers metastasize to other sites in the body, and metastasis is the leading cause of death in cancer patients. In principle, cancer cells can spread within the body by different mechanisms, such as direct invasion of surrounding tissues (per continuitatem), spread via the blood vascular system (hematogenous metastasis) and spread via the lymphatic system (lymphatic metastasis). Tumor cells can invade either the blood or lymphatic vessels to access the general circulation and then establish themselves in other tissues. Clinicopathological data suggest that the lymphatics are an initial route for the spread of solid tumors. Infiltration of lymphatic vessels by tumor cells has been found at the periphery of many experimental and human tumors, and the lymphatic system has been recognized as a conduit for tumor cell dissemination. Though the significance of angiogenesis for tumor progression has been well documented, the molecular mechanisms regulating the growth and function of lymphatic vessels are largely unknown.

Vascular endothelial growth factors, first identified in 1989, are well-known angiogenic agents and targets for anti-cancer therapies. Now it appears that VEGF-C, one recently-cloned member of the vascular endothelial growth factor (VEGF) family, is also involved in developmental and tumor-induced lymphangiogenesis. VEGF signals through two tyrosine kinase receptors, VEGFR-1 and VEGFR-2, which are expressed predominantly but not exclusively on vascular endothelial cells. As neither VEGFR-1 nor VEGFR-2 appears to be highly expressed in lymphatic endothelium, it was not surprising that a third VEGF receptor, VEGFR-3, was found to be predominantly expressed on lymphatic vessels during development. What was surprising, however, was that VEGF was not found to bind to VEGFR-3. Instead, VEGF-C was discovered to be ligand for VEGFR-3. Research groups provide direct evidence that VEGF-C is not only an important regulator of lymph vessel growth (lymphangiogenesis) in vivo but it also enhances lymphatic metastasis. Using experimental approaches, Mäkinen et al., Skobe et al., as well as Mandriota et al. demonstrate an important role of VEGFR-3 and its ligand, VEGF-C, in developmental and tumor-induced lymphangiogenesis. In normal adult human tissues, the VEGF-C receptor VEGFR-3 (FLT-4) is predominantly expressed by lymphatic endothelia. Expression of VEGF-C occurs in a variety of human tumors such as breast, colon, lung, thyroid, gastric, squamous cell cancers, mesotheliomas, neuroblastomas, sarcomas and melanomas. Moreover, expression of VEGF-C mRNA has recently been shown to correlate with the rate of metastasis to lymph nodes in breast, colorectal, gastric, thyroid, lung and prostate cancers. To date, however, lymphangiogenesis has not been causally linked to tumor metastasis.

Cyclooxygenase-2 (COX-2) enzyme catalyzes the synthesis of prostaglandins. COX-2 is an immediate-early response gene induced by inflammation, growth factors, tumor promoters, oncogenes, and carcinogens. Increased levels of COX-2 may contribute to carcinogenesis by modulating xenobiotic metabolism, apoptosis, immune surveillance, and angiogenesis. Any significant increase in tumor mass must be preceded by an increase in vascular supply to deliver nutrients and oxygen to the tumor. Recently, levels of COX-2 were found to correlate with both VEGF expression and tumor vascularization in HNSCC. This finding in human tissues is consistent with prior evidence that overexpression of COX-2 in epithelial cells led to enhanced production of VEGF and the formation of capillary-like networks. Although COX-2 contributes to the regulation of angiogenesis, its role in lymphangiogenesis is not clear.

IL-6 is a secreted, multifunctional glycoprotein. Through binding to α-chain (IL-6-R, gp80) and subsequently recruiting the β-chain (gp130) of the receptor, IL-6 performs various biological functions. The diversity of IL-6 signaling mediated via gp130 explains its functional pleiotropy. IL-6 regulates inflammatory reactions, immune responses, hepatic acute-phase protein synthesis, and several other important physiological processes. Interestingly, the influence of IL-6 in human cancers is varied depending on the cell types. For example, IL-6 has been demonstrated to promote growth of multiple myeloma, Kaposi's sarcoma, and prostatic cancer cells, while inhibiting the proliferation of lung and breast cancer cells. Previous investigations have confirmed that IL-6 is important in both physiological and pathological angiogenesis. Additionally, recent study supports the hypothesis that IL-6 facilitates tumorigenesis of cervical cancer via VEGF-mediated angiogenesis. Nevertheless, whether IL-6 could regulate the expression of VEGF-C and what is its role in lymphangiogenesis still need to be clarified.

Inhibition of angiogenesis is currently considered one of the most promising therapeutic strategies to inhibit cancer growth because it presumably can act on any tumor type, does not induce resistance of tumor cells (and can therefore be used in repeated therapeutic cycles) and has little effect on normal tissues. It now needs to be determined whether the same holds true for tumor lymphangiogenesis.

Metastases of head and neck cancers occur frequently through the lymphatic system, and the extent of lymph node involvement is a key prognostic factor for the diseases. In this study, we will conduct a systematic analysis of VEGF-C, COX-2 and IL-6 expressions and will try to find the correlation between their expressions, lymphatic metastases and patient survival. Next, we will investigate the relationship between VEGF-C, COX-2 and IL-6, and further clarify their effects on tumor growth. Undoubtedly, the findings of this study will help us understand whether lymphangiogenesis could be a focal point of anti-cancer research. If HNSCC tumors that express high levels of VEGF-C show a consistently higher incidence of lymphatic metastasis, then inhibition of VEGFR-3 function may be a novel approach to inhibit lymphatic metastasis in patients.

Study Type

Observational

Enrollment

100

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Taiwan
      • Taipei, Taiwan, 100
        • Recruiting
        • National Taiwan University Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

30 years to 75 years (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Head and neck squamous cell carcinoma

Exclusion Criteria:

  • Other pathological type

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

National Taiwan University Hospital

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

August 1, 2004

Study Registration Dates

First Submitted

September 12, 2005

First Submitted That Met QC Criteria

September 12, 2005

First Posted (ESTIMATE)

September 15, 2005

Study Record Updates

Last Update Posted (ESTIMATE)

March 30, 2006

Last Update Submitted That Met QC Criteria

March 29, 2006

Last Verified

June 1, 2005

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 9461700657

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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