Evidence map›Paper›PMID 10618428›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2000

Increased expression of preprotachykinin-I and neurokinin receptors in human breast cancer cells: implications for bone marrow metastasis.

D Singh, D D Joshi, M Hameed, J Qian, P Gascón, P B Maloof, A Mosenthal, P Rameshwar

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

53 citing papers in PubMed, 154 citations in OpenAlex.

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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

8 authors at 2 institutions in 1 country.

D SinghDepartment of Medicine-Hematology, University of Medicine and Dentistry of New Jersey-New Jersey Medical School, Newark, NJ 07103, USA.
D D Joshi
M Hameed
J Qian
P Gascón
P B Maloof
A Mosenthal
P Rameshwar
Rutgers New Jersey Medical SchoolCarnegie Mellon University · US

Funding

REGULATION OF NEUROKININ RECEPTORS IN BONE MARROW STROMAR01HL057675 · NHLBI · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI RAMESHWAR, PRANELA · 1997 to 2000
$129k
REGULATION OF HEMATOPOIESIS BY NEUROPEPTIDE SUBSTANCER01HL054973 · NHLBI · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI RAMESHWAR, PRANELA · 1995 to 1997
–
REGULATION OF NEUROKININ RECEPTORS IN BONE MARROW STROMAR29HL057675 · NHLBI · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI RAMESHWAR, PRANELA · 1996 to 1997
–
NHLBI NIH HHS HL54973NHLBI NIH HHS HL-57675NHLBI NIH HHS R01 HL054973
6 · The paper itself

Abstract

Neuropeptides are implicated in many tumors, breast cancer (BC) included. Preprotachykinin-I (PPT-I) encodes multiple neuropeptides with pleiotropic functions such as neurotransmission, immune/hematopoietic modulation, angiogenesis, and mitogenesis. PPT-I is constitutively expressed in some tumors. In this study, we investigated a role for PPT-I and its receptors, neurokinin-1 (NK-1) and NK-2, in BC by using quantitative reverse transcription-PCR, ELISA, and in situ hybridization. Compared with normal mammary epithelial cells (n = 2) and benign breast biopsies (n = 21), BC cell lines (n = 7) and malignant breast biopsies (n = 25) showed increased expression of PPT-I and NK-1. NK-2 levels were high in normal and malignant cells. Specific NK-1 and NK-2 antagonists inhibited BC cell proliferation, suggesting autocrine and/or intercrine stimulation of BC cells by PPT-I peptides. NK-2 showed no effect on the proliferation of normal cells but mediated the proliferation of BC cells. Cytosolic extracts from malignant BC cells enhanced PPT-I translation whereas extracts from normal mammary epithelial cells caused no change. These enhancing effects may be protein-specific because a similar increase was observed for IL-6 translation and no effect was observed for IL-1alpha and stem cell factor. The data suggest that PPT-I peptides and their receptors may be important in BC development. Considering that PPT-I peptides are hematopoietic modulators, these results could be extended to understand early integration of BC cells in the bone marrow, a preferred site of metastasis. Molecular signaling transduced by PPT-I peptides and the mechanism that enhances translation of PPT-I mRNA could lead to innovative strategies for BC treatments and metastasis.

Indexed as

BenzamidesBiphenyl CompoundsBone Marrow CellsBone Marrow NeoplasmsBreast NeoplasmsCell DivisionFemaleGene Expression Regulation, NeoplasticHumansIn Situ HybridizationNeurokinin-1 Receptor AntagonistsPiperidinesProtein PrecursorsReceptors, Neurokinin-1Receptors, Neurokinin-2Substance PBenzamidesBiphenyl CompoundsCP 96345Neurokinin-1 Receptor AntagonistsPiperidinespreprotachykininProtein PrecursorsReceptors, Neurokinin-1Receptors, Neurokinin-2SR 48968Substance PTachykinins

Identifiers

PMID10618428
PMCPMC26673
OpenAlexW2111723542

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.