Evidence map›Paper›PMID 1329682›Full record

ArticleAnnals of surgery1992

Neurotensin expression and release in human colon cancers.

B M Evers, J Ishizuka, D H Chung, C M Townsend, J C Thompson

Open access · greenAbstract read
In one paragraph

Article in Annals of surgery, 1992. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.0field-weighted citation impact, top 27% 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

21 citing papers in PubMed, 42 citations in OpenAlex.

  1. Review
  2. Neurotensin differentially regulates bile acid metabolism and intestinal FXR-bile acid transporter axis in response to nutrient abundance.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2021
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  19. The neurotensin gene is a downstream target for Ras activation.The Journal of clinical investigation · 1995
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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

5 authors at 1 institution in 1 country.

B M EversDepartment of Surgery, University of Texas Medical Branch, Galveston 77550.
J Ishizuka
D H Chung
C M Townsend
J C Thompson
The University of Texas Medical Branch at Galveston · US

Funding

TISSUE CULTURE COREP01DK035608 · NIDDK · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI HELLMICH, MARK R · 1986 to 2010
$14.0M
Surgical Studies of Ontogeny, Aging and the GutR37AG010885 · NIA · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI EVERS, BERNARD MARK · 2002 to 2011
$3.6M
SURGICAL STUDIES ON METABOLISM OF GI HORMONESR01DK015241 · NIDDK · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI GOMEZ, GUILLERMO · 1994 to 2003
$1.8M
SURGICAL STUDIES OF ONTOGENY, AGING AND THE GUTR01AG010885 · NIA · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI EVERS, BERNARD MARK · 1997 to 2001
$498k
SURGICAL STUDIES OF ONTOGENY, AGING AND THE GUTR29AG010885 · NIA · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI EVERS, BERNARD MARK · 1992 to 1996
–
SURGICAL STUDIES ON METABOLISM OF G. I. HORMONESR37DK015241 · NIDDK · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI THOMPSON, JAMES C · 1986 to 1993
–
NIA NIH HHS AG 10885NIDDK NIH HHS DK 15241NIDDK NIH HHS P01 DK 35608
6 · The paper itself

Abstract

Neurotensin (NT), a distal gut peptide released by intraluminal fats, is trophic for normal small bowel and colonic mucosa. In addition, NT stimulates growth of certain colon cancers; the mechanism for this effect is not known. The purpose of this study was to determine whether human colon cancers (HCC) (1) express the mRNA for NT/neuromedin N (N), (2) produce NT peptide, and (3) express the mRNA for a functional NT receptor (NTR). RNA was extracted from four HCC cell lines in culture, nine HCC lines established in athymic nude mice, and from six HCC and adjacent normal mucosa from freshly resected operative specimens; the RNA was analyzed for NT/N mRNA by Northern hybridization with a complementary DNA probe. Neurotensin peptide content, NTR expression, and intracellular Ca++ ([Ca++]i) mobilization in response to NT were evaluated in three HCC cell lines (LoVo, HT29, HCT116). Neurotensin/N mRNA transcripts were identified in all four of the HCC cell lines and in one of nine HCC in nude mice. Neurotensin expression was found in two of six freshly resected HCC and in none of the six corresponding samples of normal mucosa. Neurotensin peptide was identified by RIA in LoVo, HT29, and HCT116. In addition, NTR mRNA was found in HT29 and HCT116. Neurotensin stimulated [Ca++]i mobilization in HCT116 (without serum) and in LoVo (with 0.25% serum). These findings demonstrate the presence of NT/N mRNA and NT peptide and the presence of a functional NTR in certain HCC. Neurotensin, a potent trophic factor for normal gut mucosa, may function as an autocrine growth factor in certain human colon cancers.

Indexed as

8-Bromo Cyclic Adenosine MonophosphateAnimalsArginineCalciumColonic NeoplasmsHumansMiceMice, NudeNeurotensinReceptors, NeurotensinReceptors, NeurotransmitterRNA, MessengerTumor Cells, Cultured8-Bromo Cyclic Adenosine MonophosphateArginineCalciumNeurotensinReceptors, NeurotensinReceptors, NeurotransmitterRNA, Messenger

Identifiers

PMID1329682
PMCPMC1242644
OpenAlexW2023841298

What OpenQuestion holds

Textmetadata
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.