Evidence map›Paper›PMID 22655796›Full record

ArticleCancer biotherapy & radiopharmaceuticals2012

High-mobility group boxes mediate cell proliferation and radiosensitivity via retinoblastoma-interaction-dependent and -independent mechanisms.

Li-Li Wang, Qing-Hui Meng, Yang Jiao, Jia-Ying Xu, Chun-Min Ge, Ju-Ying Zhou, Eliot M Rosen, Hai-Chao Wang, Sai-Jun Fan

Abstract read
In one paragraph

Article in Cancer biotherapy & radiopharmaceuticals, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 23% 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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 28 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. High Mobility Group Proteins in Sepsis.Frontiers in immunology · 2022
    Review
  7. Targeting HMGB1: An available Therapeutic Strategy for Breast Cancer Therapy.International journal of biological sciences · 2022
    Review
  8. Review
  9. Article
  10. MicroRNAs in Cardiac Hypertrophy.International journal of molecular sciences · 2019
    Review
  11. [Clinical application of high mobility group box nuclear protein 1 subcomponent in the progression of liver cancer].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2018
    Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. HMGB1 in health and disease.Molecular aspects of medicine · 2014
    Review
  17. Article
  18. Article
  19. 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

9 authors at 3 institutions in 2 countries.

Li-Li WangDepartment of Radiotherapy, The First Affiliated Hospital of Soochow University, Suzhou, China.
Qing-Hui Meng
Yang Jiao
Jia-Ying Xu
Chun-Min Ge
Ju-Ying Zhou
Eliot M Rosen
Hai-Chao Wang
Sai-Jun Fan
Soochow University · CNGeorgetown University · USGeorgetown University Medical Center · US

Funding

Mechanisms of Novel Herbal Therapies for Sepsis.R01AT005076 · NCCIH · FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH · PI WANG, HAICHAO · 2010 to 2023
$4.3M
Regulation of HMGB1 Release in Endotoxemia.R01GM063075 · NIGMS · NORTH SHORE UNIVERSITY HOSPITAL · PI WANG, HAICHAO · 2002 to 2020
$4.2M
NCCIH NIH HHS R01 AT005076NCCIH NIH HHS R01AT05076NIGMS NIH HHS R01 GM063075NIGMS NIH HHS R01GM063075
6 · The paper itself

Abstract

Our previous studies have shown that high-mobility group box 1 (HMGB1) could physically associate with the retinoblastoma (RB) protein via an LXCXE (leucine-X-cysteine-X-glutamic; X=any amino acid) motif. An identical LXCXE motif is present in the HMGB1-3 protein sequences, whereas a near-consensus LXCXD (leucine-X-cysteine-X-asparagine; X=any amino acid) motif is found in the HMGB4 protein. In this study, we have demonstrated that like HMGB1, HMGB2-3 also associated with the RB in vitro and in vivo, as evidenced by glutathione-s-transferase capture and immunoprecipitation-Western blot assays. A point mutation of the LXCXE or LXCXD motif led to disruption of RB:HMGB1-4 interactions. Enforced expression of HMGB1-3 or HMGB4 by adenoviral-vector-mediated gene transfer resulted in significant inhibition of breast cancer cell proliferation through an LXCXE- or LXCXD-dependent mechanism and an increased radiosensitivity through an LXCXE- or LXCXD-independent mechanism. These results suggest an important role of the LXCXE/D motif in RB:HMGB1-4 association and modulation of cancer cell growth, but not radiosensitivity.

Indexed as

Amino Acid SequenceBinding SitesBreast NeoplasmsCell Growth ProcessesCell Line, TumorFemaleHigh Mobility Group ProteinsHumansMolecular Sequence DataProtein BindingRadiation ToleranceRetinoblastomaRetinoblastoma ProteinTransfectionHigh Mobility Group ProteinsRetinoblastoma Protein

Identifiers

PMID22655796
PMCPMC3375072
OpenAlexW2007894968

What OpenQuestion holds

Textmetadata
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.