Evidence map›Paper›PMID 27816967›Full record

ArticleOncotarget2016

Ubenimex attenuates acquired sorafenib resistance in renal cell carcinoma by inhibiting Akt signaling in a lipophagy associated mechanism.

Shuai Liu, Mingwei Gao, Xiaoqing Wang, Sentai Ding, Jiaju Lv, Dexuan Gao, Zhiyang Wang, Zhihong Niu

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.9field-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

11 citing papers in PubMed, 19 citations in OpenAlex.

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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 at 2 institutions in 1 country.

Shuai LiuDepartment of Urology, Shandong Provincial Hospital Affiliated to Shandong University, Jinan, 250021, China.
Mingwei GaoDepartment of Urology, Shandong Provincial Hospital Affiliated to Shandong University, Jinan, 250021, China.
Xiaoqing WangDepartment of Urology, Shandong Provincial Hospital Affiliated to Shandong University, Jinan, 250021, China.
Sentai DingDepartment of Urology, Shandong Provincial Hospital Affiliated to Shandong University, Jinan, 250021, China.
Jiaju LvDepartment of Urology, Shandong Provincial Hospital Affiliated to Shandong University, Jinan, 250021, China.
Dexuan GaoDepartment of Urology, Shandong Provincial Hospital Affiliated to Shandong University, Jinan, 250021, China.
Zhiyang WangDepartment of Urology, Shandong Provincial Hospital Affiliated to Shandong University, Jinan, 250021, China.
Zhihong NiuDepartment of Urology, Shandong Provincial Hospital Affiliated to Shandong University, Jinan, 250021, China.
Shandong University · CNShandong Provincial Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sorafenib is used as first line treatment of renal cell carcinoma (RCC) due to the poor sensitivity to radiotherapy and chemotherapy of this malignancy; however, acquired resistance limits the application of sorafenib and its analogues. In this study, we explored a new strategy to overcome acquired resistance to sorafenib. The RCC cell lines 786-O and ACHN were cultured in presence of increasing concentrations of sorafenib to generate sorafenib-resistant cell lines, 786-O-R and ACHN-R. Interestingly, treatment with ubenimex (0.25 mg/ml) and 3-MA (2 mM) restored the sensitivity of resistant cell lines to sorafenib, indicating the involvement of autophagy in acquired resistance. High levels of autophagy flux were observed in resistant cells, and the opposite effects of ubenimex and 3-MA suggested a complex role for autophagy. While 3-MA abolished protection in sorafenib-resistant cells, ubenimex induced uncontrolled autophagy and autophagic cell death. Lipophagy, characterized by a lipid droplet cargo, was observed in RCC tissues and cells. In sorafenib-resistant cells, ubenimex inhibited the Akt signaling pathway that regulates autophagy. In summary, lipophagy participates in sorafenib-resistance of RCC, which could be reversed by interventions targeting the Akt pathway.

Indexed as

AdenineAnimalsAutophagyCarcinoma, Renal CellCell Line, TumorDose-Response Relationship, DrugDrug Resistance, NeoplasmFemaleGene Expression Regulation, NeoplasticHumansKidney NeoplasmsLeucineLipid MetabolismMiceNiacinamidePhenylurea Compounds3-methyladenineAdenineLeucineNiacinamidePhenylurea CompoundsProto-Oncogene Proteins c-aktSorafenibubenimexAkt pathwaylipophagyrenal cell carcinomasorafenib resistanceubenimex

Identifiers

PMID27816967
PMCPMC5346704
OpenAlexW2548910306

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.