Evidence map›Paper›PMID 32393791›Full record

ArticleCell death & disease2020

The therapeutic value of SC66 in human renal cell carcinoma cells.

Ming Xu, Yin Wang, Li-Na Zhou, Li-Jun Xu, Zhi-Chang Jin, Dong-Rong Yang, Min-Bin Chen, Jin Zhu

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

16 citing papers in PubMed, 25 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 3 institutions in 1 country.

Ming Xu *Department of Urology, The Second Affiliated Hospital of Soochow University, Suzhou, China.
Yin Wang *Institute of Neuroscience, Soochow University, Suzhou, China.
Li-Na Zhou *Department of Radiotherapy and Oncology, Affiliated Kunshan Hospital of Jiangsu University, Suzhou, China.
Li-Jun Xu *Department of Urology, The Second Affiliated Hospital of Soochow University, Suzhou, China.
Zhi-Chang JinDepartment of Urology, Ningbo Urology Nephrology Hospital, Ningbo, China.
Dong-Rong YangDepartment of Urology, The Second Affiliated Hospital of Soochow University, Suzhou, China. doc_ydr@163.com.
Min-Bin ChenDepartment of Radiotherapy and Oncology, Affiliated Kunshan Hospital of Jiangsu University, Suzhou, China. cmb1981@163.com.
Jin ZhuDepartment of Urology, The Second Affiliated Hospital of Soochow University, Suzhou, China. urologistzhujin@163.com.
Second Affiliated Hospital of Soochow University · CNJiangsu University · CNSoochow University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The PI3K-AKT-mTOR cascade is required for renal cell carcinoma (RCC) progression. SC66 is novel AKT inhibitor. We found that SC66 inhibited viability, proliferation, migration and invasion of RCC cell lines (786-O and A498) and patient-derived primary RCC cells. Although SC66blocked AKT-mTORC1/2 activation in RCC cells, it remained cytotoxic in AKT-inhibited/-silenced RCC cells. In RCC cells, SC66 cytotoxicity appears to occur via reactive oxygen species (ROS) production, sphingosine kinase 1inhibition, ceramide accumulation and JNK activation, independent of AKT inhibition. The ROS scavenger N-acetylcysteine, the JNK inhibitor (JNKi) and the anti-ceramide sphingolipid sphingosine-1-phosphate all attenuated SC66-induced cytotoxicity in 786-O cells. In vivo, oral administration of SC66 potently inhibited subcutaneous 786-O xenograft growth in SCID mice. AKT-mTOR inhibition, SphK1 inhibition, ceramide accumulation and JNK activation were detected in SC66-treated 786-O xenograft tumors, indicating that SC66 inhibits RCC cell progression through AKT-dependent and AKT-independent mechanisms.

Indexed as

AnimalsAntineoplastic AgentsCarcinoma, Renal CellCell Line, TumorCell MovementCell ProliferationCyclohexanonesFemaleHumansJNK Mitogen-Activated Protein KinasesKidney NeoplasmsMice, SCIDNeoplasm InvasivenessPhosphatidylinositol 3-KinasePhosphotransferases (Alcohol Group Acceptor)Protein Kinase InhibitorsAKT1 protein, humanAntineoplastic AgentsCyclohexanonesJNK Mitogen-Activated Protein KinasesMTOR protein, humanPhosphatidylinositol 3-KinasePhosphotransferases (Alcohol Group Acceptor)Protein Kinase InhibitorsProto-Oncogene Proteins c-aktPyridinesReactive Oxygen SpeciesSC-66 compoundSphingosine KinaseTOR Serine-Threonine Kinases

Identifiers

PMID32393791
PMCPMC7214466
OpenAlexW3025121694

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.