Evidence map›Paper›PMID 20624445›Full record

ReviewBiochimica et biophysica acta2010

TBX2 and TBX3: the special value for anticancer drug targets.

Juan Lu, Xiang-Ping Li, Qi Dong, Hsiang-Fu Kung, Ming-Liang He

Open access · greenAbstract readReview
In one paragraph

Review in Biochimica et biophysica acta, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

39 citing papers in PubMed, 59 citations in OpenAlex.

  1. Review
  2. A Darwinian Perspective on Tumor Evolution.International journal of biological sciences · 2026
    Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Role of T-box transcription factor 3 in gastric cancers.World journal of gastrointestinal pathophysiology · 2023
    Review
  8. Wnt Signaling and Aging of the Gastrointestinal Tract.International journal of molecular sciences · 2022
    Review
  9. MicroRNA-143-3p/TBX3 Axis Represses Malignant Cell Behaviors in Bladder Cancer.Computational and mathematical methods in medicine · 2022
    Article
  10. Article
  11. Article
  12. Article
  13. Expression of TBX3 in Hepatocellular Carcinoma and Its Clinical Implication.Medical science monitor : international medical journal of experimental and clinical research · 2018
    Article
  14. Article
  15. Article
  16. The progress of early growth response factor 1 and leukemia.Intractable & rare diseases research · 2016
    Review
  17. Article
  18. Stratification based on methylation of TBX2 and TBX3 into three molecular grades predicts progression in patients with pTa-bladder cancer.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2015
    Article
  19. Article
  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

5 authors at 3 institutions in 1 country.

Juan LuDepartment of Otolaryngology-Head and Neck Surgery, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.
Xiang-Ping Li
Qi Dong
Hsiang-Fu Kung
Ming-Liang He
Chinese University of Hong Kong · CNNanfang Hospital · CNSouthern Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

TBX2 and TBX3 are members of the T-box family of transcription factors, which are implicated in embryonic development. Unlike most members of the T-box family, TBX2 and TBX3 are the only mammalian T-box factors which function as transcriptional repressors, mediated by the repression domain in the C-terminal. In addition to a role in development, recent evidence suggests that TBX2 and TBX3 are overexpressed in a number of cancers, including melanoma, breast, liver, lung, pancreas, ovarian, and cervical cancers. However, there is little information about the mechanisms for how these T-box genes contribute to tumorigenesis. Upregulation of TBX2 and TBX3 suppresses the expression of p14(ARF) and p21(CIP1) and promotes bypass of senescence through inactivation of p53 pathway. TBX2 functionally interacts with pRb, and pRb modulates TBX2 functional specificity. In addition, TBX2 is a player of Wnt signaling while TBX3 is a downstream target of the Wnt/beta-catenin pathway, and overexpression of TBX2 and TBX3 represses the expression of E-cadherin, which is demonstrated to be a prerequisite for epithelial tumor cell invasion. Moreover, TBX2 is shown to interact with EGR1 to block multiple downstream tumor suppressors. Here, we review the current knowledge on TBX2 and TBX3 in tumorigenesis and prospect their special value for development of target-based anticancer drugs.

Indexed as

Amino Acid SequenceAnimalsAntineoplastic Agentsbeta CateninEarly Growth Response Protein 1HumansMolecular Sequence DataProtein Structure, TertiaryRetinoblastoma ProteinSignal TransductionT-Box Domain ProteinsTumor Suppressor Protein p14ARFAntineoplastic Agentsbeta CateninEarly Growth Response Protein 1EGR1 protein, humanRetinoblastoma ProteinT-Box Domain Protein 2T-Box Domain ProteinsTBX3 protein, humanTumor Suppressor Protein p14ARF

Identifiers

PMID20624445
PMCPMC7127380
OpenAlexW2026571063

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.