Evidence map›Paper›PMID 31337279›Full record

ArticleOpen biology2019

Involvement of miR-4262 in paclitaxel resistance through the regulation of PTEN in non-small cell lung cancer.

Hongwen Sun, Xiaoting Zhou, Yanan Bao, Guosheng Xiong, Yue Cui, Hua Zhou

RetractedOpen access · goldAbstract readRetracted Publication
In one paragraph

Article in Open biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.0field-weighted citation impact, top 14% of its field
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

17 citing papers in PubMed, 31 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Hongwen SunDepartment of Thoracic Surgery, First Affiliated Hospital of Kunming Medical University, Kunming, Yunnan 650032, People's Republic of China.
Xiaoting ZhouClinical Medicine 2015, Second Clinical Medical College of Fujian Medical University, Quanzhou, Fujian 362000, People's Republic of China.
Yanan BaoDepartment of Thoracic Surgery, First Affiliated Hospital of Kunming Medical University, Kunming, Yunnan 650032, People's Republic of China.
Guosheng XiongDepartment of Thoracic Surgery, First Affiliated Hospital of Kunming Medical University, Kunming, Yunnan 650032, People's Republic of China.
Yue CuiDepartment of Thoracic Surgery, First Affiliated Hospital of Kunming Medical University, Kunming, Yunnan 650032, People's Republic of China.
Hua ZhouDepartment of Oncology Radiotherapy, First Affiliated Hospital of Kunming Medical University, Kunming, Yunnan 650032, People's Republic of China.
Kunming Medical University · CNFujian Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Non-small cell lung cancer (NSCLC) is considered to be the primary cause of cancer-related mortalities worldwide. Paclitaxel (PTX), either as a monotherapy or in combination with other drugs, is an alternative therapy for advanced NSCLC. However, cancer cell resistance against PTX represents a major clinical problem. This study aimed to investigate the role and underlying mechanism of miR-4262 in PTX-resistant NSCLC. The levels of miR-4262 were analysed by quantitative reverse transcription polymerase chain reaction. A luciferase reporter assay and bioinformatics were used to explore the potential target gene of miR-4262. Regulation of miR-4262 and PTEN expressions in NSCLC was conducted by transfection. PTX-resistant A549 and H1299 cells were established by stepwise screening through increasing the PTX concentration in the cultures. In vivo, tumorigenesis experiments were used to explore the effects of miR-4262 and PTX. Cell proliferation, apoptosis and cell migration were detected using a CCK-8 assay, flow cytometry and Transwell migration assay, respectively. PI3 K/Akt pathway-related proteins were detected by western blot. miR-4262 expression was significantly upregulated in NSCLC tissues and cell lines, and miR-4262 targeted PTEN. In addition, miR-4262 induced PTX chemoresistance by promoting survival and migration in A549/PTX and H1299/PTX cells. Moreover, miR-4262 expression and PI3 K/Akt signalling pathway-related proteins were upregulated and PTEN was downregulated in A549/PTX and H1299/PTX. Our results indicate that miR-4262 enhances PTX resistance in NSCLC cells through targeting PTEN and activating the PI3 K/Akt signalling pathway. The inhibition of miR-4262 expression might be an improved treatment to overcome PTX resistance in NSCLC.

Indexed as

A549 CellsAnimalsApoptosisCarcinoma, Non-Small-Cell LungCell Line, TumorDrug Resistance, NeoplasmGene Expression Regulation, NeoplasticHumansLung NeoplasmsMiceMice, NudeMicroRNAsPaclitaxelPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktPTEN PhosphohydrolasemicroRNA-4262 microRNA, humanMicroRNAsPaclitaxelPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktPTEN PhosphohydrolasePTEN protein, humanmiRNA-4262non-small cell lung cancerpaclitaxelPI3 K/Akt pathwayPTEN

Identifiers

PMID31337279
PMCPMC6685930
OpenAlexW2963986393

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.