Evidence map›Paper›PMID 29199261›Full record

ArticleFukushima journal of medical science2017

TBX19 is overexpressed in colorectal cancer and associated with lymph node metastasis.

Jin Ando, Motonobu Saito, Jun-Ichi Imai, Emi Ito, Yuka Yanagisawa, Reiko Honma, Katsuharu Saito, Kazunoshin Tachibana, Tomoyuki Momma, Shinji Ohki and 5 more

Open access · diamondAbstract read
In one paragraph

Article in Fukushima journal of medical science, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.3field-weighted citation impact, top 39% 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

9 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Review
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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

15 authors at 1 institution in 1 country.

Jin AndoDepartment of Gastrointestinal Tract Surgery, Fukushima Medical University School of Medicine.
Motonobu SaitoDepartment of Gastrointestinal Tract Surgery, Fukushima Medical University School of Medicine.
Jun-Ichi ImaiMedical-Industrial Translational Research Center, Fukushima Medical University.
Emi ItoMedical-Industrial Translational Research Center, Fukushima Medical University.
Yuka YanagisawaNippon Gene Co., Ltd.
Reiko HonmaNippon Gene Co., Ltd.
Katsuharu SaitoDepartment of Gastrointestinal Tract Surgery, Fukushima Medical University School of Medicine.
Kazunoshin TachibanaDepartment of Breast Surgery, Fukushima Medical University School of Medicine.
Tomoyuki MommaDepartment of Gastrointestinal Tract Surgery, Fukushima Medical University School of Medicine.
Shinji OhkiDepartment of Gastrointestinal Tract Surgery, Fukushima Medical University School of Medicine.
Tohru OhtakeDepartment of Breast Surgery, Fukushima Medical University School of Medicine.
Shinya WatanabeMedical-Industrial Translational Research Center, Fukushima Medical University.
Satoshi WaguriDepartment of Anatomy and Histology, Fukushima Medical University School of Medicine.
Koji KonoDepartment of Gastrointestinal Tract Surgery, Fukushima Medical University School of Medicine.
Seiichi TakenoshitaDepartment of Gastrointestinal Tract Surgery, Fukushima Medical University School of Medicine.
Fukushima Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The T-box 19 (TBX19) gene encodes a transcription factor characterized by a highly conserved DNA-binding motif (T-box). Recent studies have revealed that TBX19 has been identified as one of the genes activated by KRAS mutations, and is upregulated in colon adenoma. These results indicate that TBX19 may work as an oncogene in colorectal cancer (CRC). However, the expression and role of TBX19 have yet to be investigated. Here, we investigated TBX19 mRNA and protein expressions in colon cancer cells or surgically resected CRC. We found that TBX19 mRNA expression was significantly increased in tumorous tissues compared to that in non-tumorous tissues, and increased TBX19 mRNA expression was associated with positive lymph node metastasis in our cohort. The expression of TBX19 mRNA was not correlated with that of TBX19 protein in tissue sample taken from the CRC patients. Moreover, TBX19 showed positive staining even in the normal colonic tissues and the adjacent non-tumorous tissues. These results suggest that the expression of TBX19 protein is not correlated with the expression of TBX19 mRNA. In addition, our results promote further investigations into the impact of TBX19 upregulation on colorectal carcinogenesis, as well as the underlying mechanisms.

Indexed as

AdultAgedCell Line, TumorColorectal NeoplasmsFemaleHomeodomain ProteinsHumansLymphatic MetastasisMaleMiddle AgedMutationProto-Oncogene Proteins p21(ras)RNA, MessengerT-Box Domain ProteinsHomeodomain ProteinsKRAS protein, humanProto-Oncogene Proteins p21(ras)RNA, MessengerT-Box Domain ProteinsTBX19 protein, humancolorectal cancercytoplasmic granular signaldiagnostic biomarkerlymph node metastasisTBX19

Identifiers

PMID29199261
PMCPMC5792498
OpenAlexW2772578003

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.