Evidence map›Paper›PMID 32608200›Full record

ArticleYonsei medical journal2020

mTOR Signaling Combined with Cancer Stem Cell Markers as a Survival Predictor in Stage II Colorectal Cancer.

Ji Young Chang, Jae Hyun Kim, Joyeon Kang, Yehyun Park, Soo Jung Park, Jae Hee Cheon, Won Ho Kim, Hoguen Kim, Jae Jun Park, Tae Il Kim

Open access · goldAbstract read
In one paragraph

Article in Yonsei medical journal, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
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  4. Review
  5. Review
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 at 1 institution in 1 country.

Ji Young ChangDepartment of Internal Medicine and Institute of Gastroenterology, Yonsei University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-7951-456X
Jae Hyun KimDepartment of Internal Medicine and Institute of Gastroenterology, Yonsei University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-4272-8003
Joyeon KangDepartment of Internal Medicine and Institute of Gastroenterology, Yonsei University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-0256-7727
Yehyun ParkDepartment of Internal Medicine and Institute of Gastroenterology, Yonsei University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0001-8811-0631
Soo Jung ParkDepartment of Internal Medicine and Institute of Gastroenterology, Yonsei University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0003-0699-6809
Jae Hee CheonDepartment of Internal Medicine and Institute of Gastroenterology, Yonsei University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-2282-8904
Won Ho KimDepartment of Internal Medicine and Institute of Gastroenterology, Yonsei University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-5682-9972
Hoguen KimDepartment of Pathology, Yonsei University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-7444-2771
Jae Jun ParkDepartment of Internal Medicine and Institute of Gastroenterology, Yonsei University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0001-9974-1658
Tae Il KimDepartment of Internal Medicine and Institute of Gastroenterology, Yonsei University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0003-4807-890X
Yonsei University · KR

Funding

Korea Health Industry Development Institute HI14C1324National Research Foundation of Korea 2013R1A1A2010733Yonsei University College of Medicine 6-2018-0059
6 · The paper itself

Abstract

purposeWnt and mammalian target of rapamycin (mTOR) are major molecular signaling pathways associated with the development and progression of tumor, as well as the maintenance and proliferation of cancer stem cells (CSCs), in colorectal cancer (CRC). Identifying patients at risk of poor prognosis is important to determining whether to add adjuvant treatment in stage II CRC and thus improve survival. In the present study, we evaluated the prognostic value of Wnt, mTOR, and CSC markers as survival predictors in stage II CRC. MATERIALS AND

methodsWe identified 148 cases of stage II CRC and acquired their tumor tissue. Tissue microarrays for immunohistochemical staining were constructed, and the expressions of CD166, CD44, EphB2, β-catenin, pS6 were evaluated using immunohistochemical staining.

resultsThe expressions of CD166 (

conclusionSpecific combinations of CSC markers and β-catenin/mTOR signaling could be a significant predictor of poor survival in stage II CRC.

Indexed as

Antigens, CDbeta CateninBiomarkers, TumorColonic NeoplasmsColorectal NeoplasmsDisease-Free SurvivalFemaleHumansHyaluronan ReceptorsMaleMiddle AgedNeoplasm StagingNeoplastic Stem CellsPrognosisSignal TransductionTOR Serine-Threonine KinasesAntigens, CDbeta CateninBiomarkers, TumorCD44 protein, humanCTNNB1 protein, humanHyaluronan ReceptorsMTOR protein, humanTOR Serine-Threonine Kinasescarcinogenesiscolorectal cancerNeoplastic stem cellprognosissurvival

Identifiers

PMID32608200
PMCPMC7329744
OpenAlexW3038282749

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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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.