Evidence map›Paper›PMID 17465446›Full record

ArticleWorld journal of gastroenterology2007

Histopathological and genetic differences between polypoid and non-polypoid submucosal colorectal carcinoma.

Ichiro Hirata, Fang-Yu Wang, Mitsuyuki Murano, Takuya Inoue, Ken Toshina, Takashi Nishikawa, Kentaro Maemura

Abstract readComparative Study
In one paragraph

Article in World journal of gastroenterology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

1 citing paper in PubMed.

  1. 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

7 authors.

Ichiro HirataDepartment of Gastroenterology, Fujita Health University, 1-98 Dengakugakubo Katsukage-Cho, Toyoake, Aichi 470-1192, Japan. ihirata@fujita-hu.ac.jp
Fang-Yu Wang
Mitsuyuki Murano
Takuya Inoue
Ken Toshina
Takashi Nishikawa
Kentaro Maemura

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo investigate the histopathological and genetic differences between polypoid growth (PG) and non-polypoid growth (NPG) submucosal invasive colorectal carcinoma (CRC).

methodsA total of 96 cases of submucosal CRC were divided into two groups according to their growth type; 60 cases of PG and 36 cases of NPG. The size, histological degree of dysplasia, depth of submucosal invasion and lymph node metastasis were compared between the two groups. Furthermore, expression of p53 was detected by immunohistochemical staining, and K-ras gene mutation was examined by polymerase chain reaction based single-strand conformation polymorphism (SSCP).

resultsThe average size of the lesions in the NPG group was significantly smaller than those in the PG group (7.5 mm vs 13.8 mm, P<0.001). The histological degree of dysplasia tended to be more severe in NPG group, while the incidence of submucosal massive invasion and the lymph node metastasis were both significantly higher in the NPG type than in the PG group (64.3% vs 43.3%, P=0.004; 43% vs 7%, P=0.008, respectively). In addition, K-ras gene mutations were detected in 67% of lesions in the PG group, but none in the NPG group, while no difference in p53 immunohistochemical expression was found between the two groups.

conclusionCompared with PG submucosal CRC, NPG type demonstrates more frequent submucosal massive invasion, more lymph node metastasis and a higher degree dysplasia. Genetically, NPG type shows much less frequent K-ras mutation.

Indexed as

Cell ProliferationAdenocarcinomaAdenomaCarcinomaColorectal NeoplasmsDiagnosis, DifferentialDisease ProgressionGene Expression Regulation, NeoplasticHumansLymphatic MetastasisMutationPolymorphism, Single-Stranded ConformationalProto-Oncogene Proteins p21(ras)Tumor Suppressor Protein p53Proto-Oncogene Proteins p21(ras)Tumor Suppressor Protein p53

Identifiers

PMID17465446
PMCPMC4319123

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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.