Evidence map›Paper›PMID 33198792›Full record

ArticleJournal of experimental & clinical cancer research : CR2020

Inhibition of SIRT6 potentiates the anti-tumor effect of doxorubicin through suppression of the DNA damage repair pathway in osteosarcoma.

Zhongkai Zhang, Sang Hoon Ha, Young Jae Moon, Usama Khamis Hussein, Yiping Song, Kyoung Min Kim, See-Hyoung Park, Ho Sung Park, Byung-Hyun Park, Ae-Ri Ahn and 4 more

Open access · goldAbstract read
In one paragraph

Article in Journal of experimental & clinical cancer research : CR, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

24 citing papers in PubMed, 35 citations in OpenAlex.

  1. Review
  2. The SIRT Family: Subcellular Localization and Main Functions.International journal of molecular sciences · 2026
    Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Special Issue "Osteosarcomas: Treatment Strategies".Pharmaceuticals (Basel, Switzerland) · 2023
    Article
  11. Article
  12. Translational cancer research · 2023
    Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Review
  18. HBV Promotes the Proliferation of Liver Cancer Cells through the hsa_circ_0000847/miR-135a Pathway.Evidence-based complementary and alternative medicine : eCAM · 2022
    Article
  19. Review
  20. 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

14 authors at 4 institutions in 2 countries.

Zhongkai ZhangDepartment of Orthopedic Surgery, Jeonbuk National University Medical School, Jeonju, Republic of Korea.
Sang Hoon HaDivision of Biotechnology, Jeonbuk National University, Iksan, Republic of Korea.
Young Jae MoonDepartment of Biochemistry and Molecular Biology, Jeonbuk National University Medical School, Jeonju, Republic of Korea.
Usama Khamis HusseinResearch Institute of Clinical Medicine of Jeonbuk National University-Biomedical Research Institute of Jeonbuk National University Hospital and Research Institute for Endocrine Sciences, Jeonju, Republic of Korea.
Yiping SongDepartment of Orthopedic Surgery, Jeonbuk National University Medical School, Jeonju, Republic of Korea.
Kyoung Min KimResearch Institute of Clinical Medicine of Jeonbuk National University-Biomedical Research Institute of Jeonbuk National University Hospital and Research Institute for Endocrine Sciences, Jeonju, Republic of Korea.
See-Hyoung ParkDepartment of Bio and Chemical Engineering, Hongik University, Sejong, Republic of Korea.
Ho Sung ParkResearch Institute of Clinical Medicine of Jeonbuk National University-Biomedical Research Institute of Jeonbuk National University Hospital and Research Institute for Endocrine Sciences, Jeonju, Republic of Korea.
Byung-Hyun ParkDepartment of Biochemistry and Molecular Biology, Jeonbuk National University Medical School, Jeonju, Republic of Korea.
Ae-Ri AhnDepartment of Pathology, Jeonbuk National University Medical School, Jeonju, Republic of Korea.
Sang-A LeeDepartment of Pathology, Jeonbuk National University Medical School, Jeonju, Republic of Korea.
Su Jin AhnDepartment of Biochemistry and Molecular Biology, Jeonbuk National University Medical School, Jeonju, Republic of Korea.
Jung Ryul KimDepartment of Orthopedic Surgery, Jeonbuk National University Medical School, Jeonju, Republic of Korea. jrkeem@jbnu.ac.kr.
Kyu Yun JangResearch Institute of Clinical Medicine of Jeonbuk National University-Biomedical Research Institute of Jeonbuk National University Hospital and Research Institute for Endocrine Sciences, Jeonju, Republic of Korea. kyjang@jbnu.ac.kr.
Jeonbuk National University · KRJeonbuk National University Hospital · KRBeni-Suef University · EGHongik University · KR

Funding

Ministry of Science ICT and Future Planning 2017R1A5A2015061Ministry of Science ICT and Future Planning 2017R1E1A1A01074533
6 · The paper itself

Abstract

backgroundSIRT6 has diverse roles in cells, and the role of SIRT6 in tumorigenesis is controversial. Considering the role of SIRT6 as an inducer of DNA damage repair, it might be involved in resistance to anti-cancer therapy.

methodsWe evaluated the prognostic significance of SIRT6 in 37 osteosarcomas and investigated the therapeutic efficacy of SIRT6 on the anticancer effects of doxorubicin, olaparib, and ATM inhibitor.

resultsImmunohistochemical expression of SIRT6 was significantly associated with shorter overall survival and relapse-free survival of osteosarcoma patients, especially in patients who received adjuvant chemotherapy. In U2OS and KHOS/NP osteosarcoma cells, knock-down of SIRT6 significantly potentiated apoptotic effects of doxorubicin and SIRT6 overexpression induced resistance to doxorubicin. Moreover, SIRT6 induced the DNA damage repair pathway and SIRT6-mediated resistance to doxorubicin was attenuated by blocking the DNA damage repair pathway with olaparib and ATM inhibitor.

conclusionsThis study suggests that suppression of SIRT6 in combination with doxorubicin might be an effective modality in the treatment of osteosarcoma patients, especially for osteosarcomas with shorter survival with high expression of SIRT6.

Indexed as

AdultAnimalsApoptosisDNA DamageDoxorubicinHumansImmunohistochemistryMaleMiceMice, NudeOsteosarcomaPrognosisSirtuinsSurvival AnalysisTransfectionDoxorubicinSIRT6 protein, humanSirtuinsapoptosisDNA damagedoxorubicinOsteosarcomaSIRT6

Identifiers

PMID33198792
PMCPMC7670730
OpenAlexW3098077573

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.