LncRNA CALML3-AS1 suppresses papillary thyroid cancer progression via sponging miR-20a-5p/RBM38 axis
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Updated: Sep 28, 2025

In Vivo Inhibition of MicroRNA to Decrease Tumor Growth in Mice
Published on: August 23, 2019
Xiaozhou Zhang1,2, Xiaojian Zhang2, Qian Jia3
1Department of thyroid surgery, The First Affiliated Hospital of Zhengzhou University, No. 1 Jianshe East Road, Zhengzhou, 450000, Henan Province, China.
Background:
The incidence and mortality of thyroid cancer (TC) has been steadily rising in the past decades. It is imperative to have a better understanding of the molecular mechanisms underlying TC development and identify novel therapeutic targets. This study characterized the role of lncRNA CALML3-AS1 (CALML3-AS1) in the development of papillary thyroid cancer (PTC).
Method:
Related mRNAs expression were validated in the tumor and adjacent normal tissues from 52 PTC patients and PTC cell lines by qRT-PCR. Expression of RBM38 was detected by Western blot. We have also conducted CCK-8 and colony formation assays were used to detect the effect of CALML3-AS1 on cell proliferation, Transwell assay was utilized to evaluate cell migration and invasion, apoptosis detected by flow cytometry assay, RNA pull-down and luciferase assays were performed to validate gene predictions.
Results:
The results indicated that the expression of both CALML3A-S1 and RBM38 were significantly downregulated in PTC tissues (p < 0.01), while the expression of miR-20a-5p was increased in PTC (p < 0.01). Functionally, CALML3-AS1 overexpression inhibited PTC cell proliferation in vitro and in vivo. Mechanistically, CALML 3-AS1 sponged miR-20a-5p, which in turn leads to the suppression of RBM38 expression and PTC progression.
Conclusions:
CALML3-AS1 functions as a ceRNA for miR-20a-5p in the regulation of the expression of RBM38 in PTC. Higher level of CALML3-AS1 serves as a good prognostic indicator of survival in PTC patients. Targeting CALML3-AS1/ miR-20a-5p/RBM38 axis may represent a novel therapeutic strategy in the treatment of PTC.
Insights
Long non-coding RNA CALML3-AS1 (CALML3-AS1) acts as a tumor suppressor in papillary thyroid cancer (PTC) by regulating the miR-20a-5p/RBM38 axis. CALML3-AS1 overexpression inhibits PTC progression and serves as a positive prognostic marker.
Area of Science:
- Molecular Oncology
- Cancer Biology
Background:
- Thyroid cancer (TC) incidence and mortality are rising globally.
- Understanding TC molecular mechanisms and identifying therapeutic targets is crucial.
Purpose of the Study:
- To investigate the role of lncRNA CALML3-AS1 in papillary thyroid cancer (PTC) development.
- To elucidate the molecular mechanisms involving CALML3-AS1 in PTC.
Main Methods:
- qRT-PCR and Western blot to assess gene expression in PTC tissues and cell lines.
- Cell proliferation, migration, invasion, and apoptosis assays to evaluate CALML3-AS1 function.
- RNA pull-down and luciferase assays to confirm molecular interactions.
Main Results:
- CALML3-AS1 and RBM38 expression were significantly downregulated in PTC.
- miR-20a-5p expression was significantly upregulated in PTC.
- CALML3-AS1 overexpression inhibited PTC cell proliferation, migration, and invasion.
- CALML3-AS1 acts as a ceRNA for miR-20a-5p, suppressing RBM38 expression.
Conclusions:
- CALML3-AS1 functions as a ceRNA for miR-20a-5p, regulating RBM38 expression in PTC.
- CALML3-AS1 overexpression inhibits PTC progression.
- CALML3-AS1 is a potential prognostic biomarker for PTC.
- Targeting the CALML3-AS1/miR-20a-5p/RBM38 axis offers a novel therapeutic strategy for PTC.
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