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Updated: Feb 6, 2026

Spontaneous Murine Model of Anaplastic Thyroid Cancer
Published on: February 3, 2023
miR-335-5p targeting ICAM-1 inhibits invasion and metastasis of thyroid cancer cells
Li Luo1, Li Xia1, Binshan Zha2
1Department of Endocrinology, Institute of Endocrinology and Metabolism, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.
Abstract:
miRNAs is a kind of noncoding small RNAs with negative regulation function. Some miRNAs play a crucial role in the growth of tumor cells. In this study, we analyzed the role of miR-335-5p and its target gene intercellular adhesion molecule 1 (ICAM-1) in thyroid cancer. Real-time polymerase chain reaction (PCR) results showed that the expression level of ICAM-1 in cancer tissues was higher than that in their adjacent tissues. The expression level of ICAM-1 in papillary thyroid carcinoma was also significantly higher than that in other types of tumors. However, the expression of miR-335-5p is opposite to that of ICAM-1. In human thyroid cancer cell lines TPC-1, FTC-133, TT and human thyroid follicular cell line Nthyori 3-1, the expression level of ICAM-1 in TPC-1 was significantly higher than that of other cells, while the expression level of miR-335-5p in TPC-1 was significantly lower than that of other cells. When ICAM-1 expression was downregulated and miR-335-5p expression was upregulated in TPC-1 cells, ICAM-1 expression was upregulated and miR-335-5p expression was downregulated in FTC-133 cells, we found that ICAM-1 could promote the proliferation of thyroid cancer cells, while miR-335-5p could inhibit the proliferation of thyroid cancer cells. miR-335-5p could combine with 3'UTR of ICAM-1 by bioinformatics prediction. Luciferase reporter gene analysis and Western blotting detection further confirmed that miR-335-5p could target ICAM-1 and inhibit its expression. The expression level of miR-335-5p was downregulated, while the expression level of ICAM-1 was upregulated in thyroid cancer. This study will help us better understand the pathogenesis of thyroid cancer and provide new insights into the treatment of this disease.
Insights
MicroRNA-335-5p (miR-335-5p) inhibits thyroid cancer growth by downregulating intercellular adhesion molecule 1 (ICAM-1). This study reveals miR-335-5p as a potential therapeutic target for thyroid cancer.
Area of Science:
- Molecular Biology
- Oncology
- Biochemistry
Background:
- MicroRNAs (miRNAs) are noncoding small RNAs that regulate gene expression.
- Aberrant miRNA expression is implicated in various cancers, including thyroid cancer.
- Intercellular adhesion molecule 1 (ICAM-1) is a cell surface glycoprotein involved in cell adhesion and immune responses.
Purpose of the Study:
- To investigate the role of miR-335-5p and its target gene ICAM-1 in thyroid cancer.
- To elucidate the regulatory relationship between miR-335-5p and ICAM-1.
- To explore the potential of miR-335-5p as a therapeutic agent for thyroid cancer.
Main Methods:
- Real-time polymerase chain reaction (PCR) to quantify gene expression.
- Bioinformatics prediction to identify potential miRNA-target interactions.
- Luciferase reporter gene assay and Western blotting to validate miRNA targeting.
- In vitro cell culture experiments to assess the impact of miR-335-5p and ICAM-1 on cell proliferation.
Main Results:
- ICAM-1 expression was significantly upregulated in thyroid cancer tissues and cell lines, particularly in papillary thyroid carcinoma.
- miR-335-5p expression was inversely correlated with ICAM-1 expression.
- miR-335-5p directly targets ICAM-1, inhibiting its expression and consequently suppressing thyroid cancer cell proliferation.
- Downregulation of miR-335-5p and upregulation of ICAM-1 were observed in thyroid cancer.
Conclusions:
- miR-335-5p acts as a tumor suppressor in thyroid cancer by inhibiting ICAM-1 expression.
- The miR-335-5p/ICAM-1 axis plays a critical role in thyroid cancer pathogenesis.
- Targeting miR-335-5p offers a promising therapeutic strategy for thyroid cancer treatment.
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