AI Article Synopsis

  • The study investigates the role of Thomsen-Friedenreich antibody (TF-Ab) and its impact on thyroid cancer (TC), specifically looking at how it may inhibit tumor growth and metastasis.
  • Researchers compared TF-Ab levels in patients with primary papillary TC and found that these levels were lower than in normal individuals, with no correlation to lymph node metastasis.
  • The introduction of a specific monoclonal antibody (mAb A78-G/A7) significantly impaired TC cells' ability to adhere, invade, and migrate, indicating its potential as a therapeutic agent against thyroid cancer.

Article Abstract

Background: Thomsen-Friedenreich antibody (TF-Ab) is a specific antibody against the Thomsen-Friedenreich antigen (TF-Ag). At present, studies on a number of other tumors have shown that TF-Ab can effectively inhibit metastasis and induce apoptosis in tumor cells. However, the role of TF-Ab in thyroid cancer (TC) remains unclear.

Materials And Methods: Normal subjects and patients with primary papillary TC with or without lymph node metastasis were tested for TF-Ab expression by enzyme-linked immunosorbent assays (ELISAs). Immunofluorescence was used to assess the expression of TF-Ag in thyroid papillary carcinoma with or without lymph node metastasis and undifferentiated cancer tissues. To evaluate the role of TF-Ab in TC, the effects of TF monoclonal antibody (mAb A78-G/A7) on cell biological function were investigated by MTT assays, flow cytometry, adhesion assays and transwell experiments.

Results: Compared with normal individuals, TF-Ab levels in patients with TC were decreased, but no changes were observed with respect to lymph node metastasis. The expression of TF-Ag in TC tissues was relatively higher than that detected in adjacent tissues, but it was not affected by the presence or absence of lymph node metastasis. Upon treatment mAb A78-G/A7 treating, TC cell cycles were affected, meanwhile the abilities to adhere, invade and migrate were also significantly reduced.

Conclusion: The results of the present study showed that mAb A78-G/A7 could affect the invasion and migration of all assayed TC cell lines. The effects of mAb A78-G/A7 on the cell cycle, adhesion, invasion and migration of TC cells were more significant than those observed for proliferation and apoptosis.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7500363PMC
http://dx.doi.org/10.2147/OTT.S261685DOI Listing

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