Evidence map›Paper›PMID 28627658›Full record

ArticleMolecular medicine reports2017

Shikonin promotes adriamycin‑induced apoptosis by upregulating caspase‑3 and caspase‑8 in osteosarcoma.

Qing Yang, Suoyuan Li, Zeze Fu, Binhui Lin, Zifei Zhou, Zhuoying Wang, Yingqi Hua, Zhengdong Cai

Open access · hybridAbstract read
In one paragraph

Article in Molecular medicine reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.1field-weighted citation impact, top 16% 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

14 citing papers in PubMed, 32 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.

Qing YangDepartment of Orthopedics, Nanjing Medical University Shanghai Tenth People's Hospital, Nanjing, Jiangsu 210029, P.R. China.
Suoyuan LiDepartment of Orthopedics, Shanghai General Hospital, Nanjing Medical University, Shanghai 201600, P.R. China.
Zeze FuDepartment of Orthopedics, Shanghai General Hospital, Shanghai Jiao Tong University, Shanghai 201600, P.R. China.
Binhui LinDepartment of Orthopedics, Shanghai General Hospital, Nanjing Medical University, Shanghai 201600, P.R. China.
Zifei ZhouDepartment of Orthopedics, Shanghai General Hospital, Shanghai Jiao Tong University, Shanghai 201600, P.R. China.
Zhuoying WangDepartment of Orthopedics, Shanghai General Hospital, Shanghai Jiao Tong University, Shanghai 201600, P.R. China.
Yingqi HuaDepartment of Orthopedics, Shanghai General Hospital, Shanghai Jiao Tong University, Shanghai 201600, P.R. China.
Zhengdong CaiDepartment of Orthopedics, Nanjing Medical University Shanghai Tenth People's Hospital, Nanjing, Jiangsu 210029, P.R. China.
Nanjing Medical University · CNShanghai Jiao Tong University · CNShanghai First People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteosarcoma is the most common primary malignant bone tumor. Cancer cells employ a host of mechanisms to develop resistance to adriamycin (ADM) or other chemotherapeutic drugs. Shikonin (SK), an active constituent extracted from a Chinese medicinal herb, has been shown to cooperate with ADM in the treatment of osteosarcoma and certain other types of cancer by contributing to the response rate of chemotherapy and the side effects. The aim of the present study was to investigate the role and underlying mechanism of SK in chemotherapy for osteosarcoma. In the present study, a CCK-8 assay was performed to assess cell survival rate in vitro. Western blot analysis was performed to determine the expression levels of B‑cell lymphoma 2‑associated X protein (Bax), caspase‑3, caspase‑8, and poly (ADP‑ribose) polymerase (PARP). Flow cytometry was used to analyze cell cycle and cell death. The survival rate of cells decreased significantly in a dose‑ and time‑dependent manner when treated with a combination of SK and ADM. Western blot analysis revealed increased expression levels of Bax, caspase‑3, caspase‑8 and PARP in U2OS and MG63 cells 48 h following treatment with SK and ADM. Flow cytometric analysis showed that the combined treatment of SK and ADM significantly induced apoptosis in the osteosarcoma cells. Taken together SK cooperated with ADM to promote apoptosis, possibly by inducing caspase‑3‑ and caspase‑8‑dependent apoptosis. SK may be a potential enhancer in the treatment of drug‑resistant primary osteosarcoma.

Indexed as

Antibiotics, AntineoplasticApoptosisBone NeoplasmsCaspase 3Caspase 8Cell Line, TumorCell ProliferationCell SurvivalDoxorubicinDrug SynergismHumansNaphthoquinonesOsteosarcomaAntibiotics, AntineoplasticCaspase 3Caspase 8DoxorubicinNaphthoquinonesshikonin

Identifiers

PMID28627658
PMCPMC5562087
OpenAlexW2621415533

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.