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Updated: Oct 8, 2025

In Vivo Inhibition of MicroRNA to Decrease Tumor Growth in Mice
Published on: August 23, 2019
A ceRNA network mediated by LINC00475 in papillary thyroid carcinoma
Yarong Yang1, Wenjuan Hua1, Mei Zeng1
1Department of Nuclear Medicine, Wuhan Fourth Hospital/Puai Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, Hubei, China.
Long noncoding RNA LINC00475 promotes papillary thyroid carcinoma (PTC) progression by increasing ZCCHC12 expression. This study elucidates the LINC00475/miR-376c-3p/ZCCHC12 pathway in PTC, offering potential therapeutic targets for this common thyroid cancer.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Papillary thyroid carcinoma (PTC) is the most common differentiated thyroid cancer.
- Long noncoding RNAs (lncRNAs) are implicated in various human cancers, including PTC.
Purpose of the Study:
- To investigate the function and mechanism of lncRNA LINC00475 in papillary thyroid carcinoma.
- To identify the molecular pathway involving LINC00475 in PTC progression.
Main Methods:
- Reverse-transcription polymerase chain reaction (RT-PCR) and subcellular fractionation to determine LINC00475 expression and location.
- Cell counting kit-8, ethynyl deoxyuridine (EdU) incorporation, wound healing, and Transwell assays to assess cell proliferation, viability, migration, and invasion.
- Luciferase reporter, RNA pulldown, and RNA immunoprecipitation (RIP) assays to confirm molecular interactions.
Main Results:
- LINC00475 was upregulated in PTC cells and localized in the cytoplasm.
- LINC00475 knockdown inhibited PTC cell viability, proliferation, migration, and invasion.
- LINC00475 upregulated ZCCHC12 expression by sponging miR-376c-3p, and ZCCHC12 overexpression partially rescued the inhibitory effects of LINC00475 knockdown.
Conclusions:
- LINC00475 promotes PTC cell proliferation, migration, and invasion.
- The mechanism involves LINC00475 upregulating ZCCHC12 via interaction with miR-376c-3p.
- LINC00475 acts as a potential oncogene in PTC progression.
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