Evidence map›Paper›PMID 26933915›Full record

ArticleOncotarget2016

Antitumor effects of calgranulin B internalized in human colon cancer cells.

Kun Kim, Kyung-Hee Kim, Kangsan Roh, Byong Chul Yoo, Ja-Lok Ku, Young-Kyoung Shin, Jae Youl Cho, Minjae Kim, Myung-Hee Kwon, Sung Ho Goh and 2 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.9field-weighted citation impact, top 24% 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

6 citing papers in PubMed, 7 citations in OpenAlex.

  1. 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

12 authors at 4 institutions in 1 country.

Kun KimColorectal Cancer Branch, Research Institute, National Cancer Center, Goyang, Gyeonggi, Republic of Korea.
Kyung-Hee KimColorectal Cancer Branch, Research Institute, National Cancer Center, Goyang, Gyeonggi, Republic of Korea.
Kangsan RohColorectal Cancer Branch, Research Institute, National Cancer Center, Goyang, Gyeonggi, Republic of Korea.
Byong Chul YooColorectal Cancer Branch, Research Institute, National Cancer Center, Goyang, Gyeonggi, Republic of Korea.
Ja-Lok KuCancer Research Institute, Seoul National University College of Medicine, Seoul, Republic of Korea.
Young-Kyoung ShinCancer Research Institute, Seoul National University College of Medicine, Seoul, Republic of Korea.
Jae Youl ChoDepartment of Genetic Engineering, Sungkyunkwan University, Suwon, Republic of Korea.
Minjae KimDepartment of Microbiology, Ajou University School of Medicine, Suwon, Republic of Korea.
Myung-Hee KwonDepartment of Microbiology, Ajou University School of Medicine, Suwon, Republic of Korea.
Sung Ho GohCancer Genomics Branch, Research Institute, National Cancer Center, Goyang, Gyeonggi, Republic of Korea.
Hee Jin ChangColorectal Cancer Branch, Research Institute, National Cancer Center, Goyang, Gyeonggi, Republic of Korea.
Jae Hwan OhColorectal Cancer Branch, Research Institute, National Cancer Center, Goyang, Gyeonggi, Republic of Korea.
National Cancer Center · KRAjou University · KRSeoul National University · KRSungkyunkwan University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Calgranulin B is a small, calcium-binding protein expressed in neutrophils that is secreted into the tumor microenvironment in cancer cases. We previously showed that calgranulin B levels are increased in the stools of colorectal cancer patients. In patient tumor tissues, calgranulin B protein levels correlated with the presence of stromal inflammatory cells surrounding tumor cells, and calgranulin B promoter methylation was observed in both paired human tissues and colon cancer cell lines. Cell lines did not express calgranulin B, but in vitro studies showed that colon cancer cells internalized extracellular calgranulin B, while other types of cancer cells did not. Calgranulin B internalization led to reduced cell proliferation and increased apoptotic cell death. AKT and ERK signals were also increased after calgranulin B treatment, as were p53, β-catenin, E-cadherin and cleaved caspase-3 levels. Additionally, a human protein microarray identified aurora A kinase as a calgranulin B binding partner, and binding inhibited aurora A kinase activity in a dose-dependent manner. Our findings demonstrate the antitumor effects of calgranulin B in the inflammatory microenvironment and suggest that calgranulin B could be potentially efficacious in the treatment of colon cancer.

Indexed as

ApoptosisAurora KinasesCalgranulin BCell CycleCell ProliferationColonic NeoplasmsHumansSignal TransductionTumor Cells, CulturedTumor MicroenvironmentAurora KinasesCalgranulin Baurora A kinasecalgranulin Bcolon cancerinflammatory microenvironmentprotein internalization

Identifiers

PMID26933915
PMCPMC4991461
OpenAlexW2288904297

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.