Evidence map›Paper›PMID 26910279›Full record

ArticleOncotarget2016

Assessment of cholecystokinin 2 receptor (CCK2R) in neoplastic tissue.

Jyoti Roy, Karson S Putt, Domenico Coppola, Marino E Leon, Farah K Khalil, Barbara A Centeno, Noel Clark, Valerie E Stark, David L Morse, Philip S Low

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 23 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 3 pooled it
3.3field-weighted citation impact, top 8% 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

23 citing papers in PubMed, 3 syntheses or guidelines pooled it, 45 citations in OpenAlex.

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  6. Implicating the cholecystokinin B receptor in liver stem cell oncogenesis.American journal of physiology. Gastrointestinal and liver physiology · 2024
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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

10 authors at 2 institutions in 1 country.

Jyoti RoyCenter for Drug Discovery, Purdue University, West Lafayette, IN 47907 USA.
Karson S PuttCenter for Drug Discovery, Purdue University, West Lafayette, IN 47907 USA.
Domenico CoppolaDepartment of Anatomic Pathology, H. Lee Moffitt Cancer Center, Tampa, FL 33612 USA.
Marino E LeonDepartment of Anatomic Pathology, H. Lee Moffitt Cancer Center, Tampa, FL 33612 USA.
Farah K KhalilDepartment of Anatomic Pathology, H. Lee Moffitt Cancer Center, Tampa, FL 33612 USA.
Barbara A CentenoDepartment of Anatomic Pathology, H. Lee Moffitt Cancer Center, Tampa, FL 33612 USA.
Noel ClarkTissue Core, H. Lee Moffitt Cancer Center, Tampa, FL 33612 USA.
Valerie E StarkDepartment of Cancer Imaging and Metabolism, Imaging and Technology Center of Excellence, H. Lee Moffitt Cancer Center, Tampa, FL 33612 USA.
David L MorseDepartment of Cancer Imaging and Metabolism, Imaging and Technology Center of Excellence, H. Lee Moffitt Cancer Center, Tampa, FL 33612 USA.
Philip S LowCenter for Drug Discovery, Purdue University, West Lafayette, IN 47907 USA.
Moffitt Cancer Center · USPurdue University West Lafayette · US

Funding

TRANSLATIONAL RESEARCHP30CA076292 · NCI · UNIVERSITY OF SOUTH FLORIDA · PI KENNETH Lynn WRIGHT · 1998 to 2026
$93.5M
NCI NIH HHS P30 CA076292
6 · The paper itself

Abstract

The expression of cholecystokinin 2 receptor (CCK2R, CCKBR or gastrin receptor) has been reported on a diverse range of cancers such as colorectal, liver, lung, pancreatic, ovarian, stomach, thyroid and numerous neuroendocrine/carcinoid tumors. Some cancers of the colorectum, lung, pancreas and thyroid have been shown to overexpress CCK2R in relation to normal matched tissues of the same organ. This reported overexpression has led to the development of a number of CCK2R-ligand targeted imaging and therapeutic agents. However, no comprehensive study comparing the expression of CCK2R in multiple cancers to multiple normal tissues has been performed. Herein, we report the immunohistochemical analysis of cancer samples from gastrointestinal stromal tumor (GIST), hepatocellular carcinoma (HCC), non-small cell lung cancer (NSCLC), pancreatic adenocarcinoma, and thyroid cancer against multiple normal tissue samples from esophagus, liver, lung, pancreas, stomach, spleen and thyroid. These results show that CCK2R expression is present in nearly all cancer and normal samples tested and that none of the cancer samples had expression that was statistically greater than that of all of the normal samples.

Indexed as

Biomarkers, TumorCarcinoma, Non-Small-Cell LungCase-Control StudiesGastrointestinal Stromal TumorsGene Expression Regulation, NeoplasticHumansLung NeoplasmsNeoplasm InvasivenessNeoplasm MetastasisNeoplasmsNeoplasm StagingNeuroendocrine TumorsPancreatic NeoplasmsPrognosisReceptor, Cholecystokinin BThyroid NeoplasmsBiomarkers, TumorReceptor, Cholecystokinin BCCK2RCCKBRcholecystokinin 2 receptorgastrin receptor

Identifiers

PMID26910279
PMCPMC4924738
OpenAlexW2292943820

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.