Evidence map›Paper›PMID 9391078›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1997

SARPs: a family of secreted apoptosis-related proteins.

H S Melkonyan, W C Chang, J P Shapiro, M Mahadevappa, P A Fitzpatrick, M C Kiefer, L D Tomei, S R Umansky

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 106 papers.

0numbers the graph read from it
0cells of the map it votes in
106citing papers in PubMed
6.7field-weighted citation impact, top 2% 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

106 citing papers in PubMed, 324 citations in OpenAlex.

  1. Review
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  13. Wnts and the hallmarks of cancer.Cancer metastasis reviews · 2020
    Review
  14. Article
  15. Article
  16. Role of Sfrps in cardiovascular disease.Therapeutic advances in chronic disease · 2020
    Review
  17. Article
  18. Sfrp4 repression of the Ror2/Jnk cascade in osteoclasts protects cortical bone from excessive endosteal resorption.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  19. Article
  20. Article

46 more citing papers are in PubMed but not listed here.

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.

H S MelkonyanLXR Biotechnology, Inc., 1401 Marina Way South, Richmond, CA 94804, USA. hmelkonyan@lxr.com
W C Chang
J P Shapiro
M Mahadevappa
P A Fitzpatrick
M C Kiefer
L D Tomei
S R Umansky

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Quiescent mouse embryonic C3H/10T1/2 cells are more resistant to different proapoptotic stimuli than are these cells in the exponential phase of growth. However, the exponentially growing 10T1/2 cells are resistant to inhibitors of RNA or protein synthesis, whereas quiescent cells die upon these treatments. Conditioned medium from quiescent 10T1/2 cells possesses anti-apoptotic activity, suggesting the presence of protein(s) that function as an inhibitor of the apoptotic program. Using differential display technique, we identified and cloned a cDNA designated sarp1 (secreted apoptosis-related protein) that is expressed in quiescent but not in exponentially growing 10T1/2 cells. Hybridization studies with sarp1 revealed two additional family members. Cloning and sequencing of sarp2 and sarp3 revealed 38% and 40% sequence identity to sarp1, respectively. Human breast adenocarcinoma MCF7 cells stably transfected with sarp1 or infected with SARP1-expressing adenovirus became more resistant, whereas cells transfected with sarp2 displayed increased sensitivity to different proapoptotic stimuli. Expression of sarp family members is tissue specific. sarp mRNAs encode secreted proteins that possess a cysteine-rich domain (CRD) homologous to the CRD of frizzled proteins but lack putative membrane-spanning segments. Expression of SARPs modifies the intracellular levels of beta-catenin, suggesting that SARPs interfere with the Wnt-frizzled proteins signaling pathway.

Indexed as

Trans-ActivatorsAmino Acid SequenceAnimalsApoptosisbeta CateninCell DivisionCell LineCloning, MolecularCulture Media, ConditionedCytoskeletal ProteinsFrizzled ReceptorsGene ExpressionHumansInterphaseMiceMolecular Sequence Databeta CateninCTNNB1 protein, humanCTNNB1 protein, mouseCulture Media, ConditionedCytoskeletal ProteinsFrizzled ReceptorsFZD2 protein, humanFzd2 protein, mouseReceptors, G-Protein-CoupledReceptors, NeurotransmitterTrans-Activators

Identifiers

PMID9391078
PMCPMC28358
OpenAlexW2001372468

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.