Evidence map›Paper›PMID 26083008›Full record

ArticleCancer science2015

Assessment of elasticity of colorectal cancer tissue, clinical utility, pathological and phenotypical relevance.

Shingo Kawano, Motohiro Kojima, Yoichi Higuchi, Motokazu Sugimoto, Koji Ikeda, Naoki Sakuyama, Shinichiro Takahashi, Ryuichi Hayashi, Atsushi Ochiai, Norio Saito

Abstract read
In one paragraph

Article in Cancer science, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed
–field-weighted citation impact
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

73 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
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  9. Review
  10. Article
  11. The functional role of the extracellular matrix in inflammatory bowel disease associated gut fibrosis.Matrix biology : journal of the International Society for Matrix Biology · 2025
    Review
  12. Review
  13. Article
  14. Review
  15. Article
  16. Frontiers in genetics · 2025
    Review
  17. Article
  18. Article
  19. Article
  20. Dual and triple gene combinations of KRT5, KRT17, and S100A2 identify basal-like subtype of pancreatic ductal adenocarcinoma and correlate with survival outcome.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2024
    Article

13 more citing papers are in PubMed but not listed here.

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

10 authors.

Shingo KawanoDepartment of Colorectal and Pelvic Surgery, National Cancer Center Hospital East, Chiba, Japan.
Motohiro KojimaDivision of Pathology, Research Center for Innovative Oncology, National Cancer Center Hospital East, Chiba, Japan.
Yoichi HiguchiDivision of Pathology, Research Center for Innovative Oncology, National Cancer Center Hospital East, Chiba, Japan.
Motokazu SugimotoDepartment of Hepatobiliary-Pancreatic Surgery, National Cancer Center Hospital East, Chiba, Japan.
Koji IkedaDepartment of Colorectal and Pelvic Surgery, National Cancer Center Hospital East, Chiba, Japan.
Naoki SakuyamaDepartment of Colorectal and Pelvic Surgery, National Cancer Center Hospital East, Chiba, Japan.
Shinichiro TakahashiDepartment of Hepatobiliary-Pancreatic Surgery, National Cancer Center Hospital East, Chiba, Japan.
Ryuichi HayashiAdvanced Clinical Research of Cancer, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Atsushi OchiaiDivision of Pathology, Research Center for Innovative Oncology, National Cancer Center Hospital East, Chiba, Japan.
Norio SaitoDepartment of Colorectal and Pelvic Surgery, National Cancer Center Hospital East, Chiba, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Generally, cancer tissue is palpated as a hard mass. However, the elastic nature of cancer tissue is not well understood. The aim of the present study was to evaluate the clinical utility of measuring the elastic modulus (EM) in colorectal cancer tissue. Using a tactile sensor, we measured the EM of 106 surgically resected colorectal cancer tissues. Data on the EM were compared with clinicopathological findings, including stromal features represented by Azan staining and the α-SMA positive area ratio of the tumor area. Finally, a cDNA microarray profile of the tumors with high EM were compared with the findings of tumors with low EM. A higher EM in tumors was associated with pathological T, N, and M-stage tumors (P < 0.001, P = 0.001 and P = 0.011, respectively). Patients with high EM tumors had shorter disease-free survival than had patients with low EM. The EM showed strongly positive correlation with the Azan staining positive area ratio (r = 0.908) and the α-SMA positive area ratio (r = 0.921). Finally, the cDNA microarray data of the tumors with high EM revealed a distinct gene expression profile compared with data from those tumors with low EM. The assessment of the elasticity of colorectal cancer tissue may allow a more accurate clinical stage and prognosis estimation. The distinct phenotypical features of the high EM tumors and their strong association with stromal features suggest the existence of a biological mechanism involved in this phenomenon that may contribute to future therapy.

Indexed as

AdultAgedAged, 80 and overColorectal NeoplasmsDisease-Free SurvivalElasticityFemaleHumansMaleMiddle AgedPrognosisTranscriptomeColorectal cancerdisease-free survivalelasticitypathologicalphenotypical

Identifiers

PMID26083008
PMCPMC4582994

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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.