Evidence map›Paper›PMID 38715012›Full record

ArticleMolecular cancer2024

circ_PPAPDC1A promotes Osimertinib resistance by sponging the miR-30a-3p/ IGF1R pathway in non-small cell lung cancer (NSCLC).

Yi-Fang Tang, Zheng-Hua Liu, Lei-Yi Zhang, Sheng-Hao Shi, Shun Xu, Jin-An Ma, Chun-Hong Hu, Fang-Wen Zou

Abstract read
In one paragraph

Article in Molecular cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

34 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Circular RNAs: from transcriptional noise to engineered therapeutics.Frontiers in epigenetics and epigenomics · 2026
    Review
  9. Article
  10. PTPN9 dephosphorylates IGF1RJournal of experimental & clinical cancer research : CR · 2025
    Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. EGFR-TKIs Induced DPP4 Drives Metabolic Reprogramming of Persister Cells in Lung Cancer.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. [Expression of NFAT5 and IGF1R in nasopharyngeal carcinoma tissues and analysis of clinical characteristics].Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology head and neck surgery · 2025
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Yi-Fang TangDepartment of Anesthesiology, The Second Xiangya Hospital of Central South University, Changsha, 410000, Hunan, P.R. China.
Zheng-Hua LiuDepartment of Thoracic Surgery, The First Affiliated Hospital of China Medical University, Shenyang, 11000, Liaoning, P.R. China.
Lei-Yi ZhangDepartment of General Surgery, The Second Xiangya Hospital of Central South University, Changsha, 410000, Hunan, P.R. China.
Sheng-Hao ShiDepartment of Oncology, The Second Xiangya Hospital of Central South University, Changsha, 410000, Hunan, P.R. China.
Shun XuDepartment of Thoracic Surgery, The First Affiliated Hospital of China Medical University, Shenyang, 11000, Liaoning, P.R. China.
Jin-An MaDepartment of Oncology, The Second Xiangya Hospital of Central South University, Changsha, 410000, Hunan, P.R. China.
Chun-Hong HuDepartment of Oncology, The Second Xiangya Hospital of Central South University, Changsha, 410000, Hunan, P.R. China.
Fang-Wen ZouDepartment of Oncology, The Second Xiangya Hospital of Central South University, Changsha, 410000, Hunan, P.R. China. zoufangwen@csu.edu.cn.

Funding

National Natural Science Foundation of China No.82202923Natural Science Foundation of Changsha No.72518Soft Science Project of Changsha No.79330
6 · The paper itself

Abstract

backgroundRecent evidence has demonstrated that abnormal expression and regulation of circular RNA (circRNAs) are involved in the occurrence and development of a variety of tumors. The aim of this study was to investigate the effects of circ_PPAPDC1A in Osimertinib resistance in NSCLC.

methodsHuman circRNAs microarray analysis was conducted to identify differentially expressed (DE) circRNAs in Osimertinib-acquired resistance tissues of NSCLC. The effect of circ_PPAPDC1A on cell proliferation, invasion, migration, and apoptosis was assessed in both in vitro and in vivo. Dual-luciferase reporter assay, RT-qPCR, Western-blot, and rescue assay were employed to confirm the interaction between circ_PPAPDC1A/miR-30a-3p/IGF1R axis.

resultsThe results revealed that circ_PPAPDC1A was significantly upregulated in Osimertinib acquired resistance tissues of NSCLC. circ_PPAPDC1A reduced the sensitivity of PC9 and HCC827 cells to Osimertinib and promoted cell proliferation, invasion, migration, while inhibiting apoptosis in Osimertinib-resistant PC9/OR and HCC829/OR cells, both in vitro and in vivo. Silencing circ_PPAPDC1A partially reversed Osimertinib resistance. Additionally, circ_PPAPDC1A acted as a competing endogenous RNA (ceRNA) by targeting miR-30a-3p, and Insulin-like Growth Factor 1 Receptor (IGF1R) was identified as a functional gene for miR-30a-3p in NSCLC. Furthermore, the results confirmed that circ_PPAPDC1A/miR-30a-3p/IGF1R axis plays a role in activating the PI3K/AKT/mTOR signaling pathway in NSCLC with Osimertinib resistance.

conclusionsTherefore, for the first time we identified that circ_PPAPDC1A was significantly upregulated and exerts an oncogenic role in NSCLC with Osimertinib resistance by sponging miR-30a-3p to active IGF1R/PI3K/AKT/mTOR pathway. circ_PPAPDC1A may serve as a novel diagnostic biomarker and therapeutic target for NSCLC patients with Osimertinib resistance.

Indexed as

AcrylamidesAniline CompoundsCarcinoma, Non-Small-Cell LungCell ProliferationDrug Resistance, NeoplasmGene Expression Regulation, NeoplasticLung NeoplasmsMicroRNAsReceptor, IGF Type 1RNA, CircularSignal TransductionAnimalsApoptosisCell Line, TumorCell MovementFemaleAcrylamidesAniline CompoundsIGF1R protein, humanIndolesMicroRNAsMIRN30a microRNA, humanMIRN30b microRNA, humanosimertinibPyrimidinesReceptor, IGF Type 1RNA, Circularcirc_PPAPDC1AIGF1RmiR-30a-3pNSCLCOsimertinib resistance

Identifiers

PMID38715012
PMCPMC11075361

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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.