Evidence map›Paper›PMID 42724449›Full record

ArticleTranslational cancer research2026

CircFN1 promotes invasion of papillary thyroid carcinoma cells by activating the PI3K/AKT pathway via the miR-29a/TRIB2 axis.

Ning Zhang, Jingyan Zhang, Xiaonuo Wang, Ming Tao, Gongqi Li, Yanjiao Li, Qingyang Bai, Qiuting Wen

Abstract read
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Article in Translational cancer research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Ning ZhangDepartment of Pathology, Qiqihar Medical University, Qiqihar, China.
Jingyan ZhangDepartment of Pathology, Qiqihar Medical University, Qiqihar, China.
Xiaonuo WangDepartment of Pathology, Qiqihar Medical University, Qiqihar, China.
Ming TaoDepartment of Pathology, Qiqihar Medical University, Qiqihar, China.
Gongqi LiDepartment of Pathology, Qiqihar Medical University, Qiqihar, China.
Yanjiao LiDepartment of Pathology, Qiqihar Medical University, Qiqihar, China.
Qingyang BaiDepartment of Pathology, Qiqihar Medical University, Qiqihar, China.
Qiuting WenDepartment of Pathology, Qiqihar Medical University, Qiqihar, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Circular RNAs regulate cancer progression, but their mechanisms in papillary thyroid carcinoma (PTC) invasion remain incompletely defined. This study investigated circFN1 expression and function and examined whether circFN1 promotes PTC invasion through microRNA-29a (miR-29a)/tribbles pseudokinase 2 (TRIB2)-mediated PI3K/AKT activation. Methods: The abundance of TRIB2 and p-AKT in paired PTC and adjacent non-cancerous tissues was first assessed by immunohistochemistry (IHC), and circFN1, miR-29a, TRIB2, p-PI3K and p-AKT were further evaluated by quantitative real-time polymerase chain reaction (qRT-PCR) and Western blotting. In TPC-1 cells, circFN1 overexpression/knockdown, miR-29a overexpression/inhibition and TRIB2 overexpression models were established. Cell proliferation, colony formation, apoptosis, migration and invasion were assessed. Dual-luciferase reporter and RNA immunoprecipitation (RIP) assays were used to validate miR-29a/TRIB2 targeting and circFN1-miR-29a association. The phosphorylation status of crucial proteins within the PI3K/AKT signaling cascade (p-PI3K, p-AKT) was detected by qRT-PCR and Western Blot to confirm the activation status of this signaling axis. Results: Examination of clinical specimens indicated that the abundance of TRIB2 and p-AKT showed significant upregulation when compared with adjacent normal tissues. Additional paired-tissue validation further showed increased circFN1 and TRIB2 expression, decreased miR-29a expression, and enhanced PI3K/AKT phosphorylation in PTC tissues. Conclusions: circFN1 may promote PTC invasion through the miR-29a/TRIB2/PI3K/AKT axis. This axis represents a potential biomarker and therapeutic target for assessing invasion risk in PTC.

Indexed as

circFN1miR-29aPapillary thyroid carcinoma (PTC)PI3K/AKT signaling pathwayTRIB2

Identifiers

PMID42724449
PMCPMC13559673

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.