Evidence map›Paper›PMID 8080043›Full record

ArticleThe American journal of pathology1994

Osteopontin expression and distribution in human carcinomas.

L F Brown, A Papadopoulos-Sergiou, B Berse, E J Manseau, K Tognazzi, C A Perruzzi, H F Dvorak, D R Senger

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In one paragraph

Article in The American journal of pathology, 1994. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 109 papers.

0numbers the graph read from it
0cells of the map it votes in
109citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

109 citing papers in PubMed, 328 citations in OpenAlex.

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  19. Cancer Secretome May Influence BSP and DSP Expression in Human Salivary Gland Cells.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2017
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49 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 at 1 institution in 1 country.

L F BrownDepartment of Pathology, Beth Israel Hospital, Boston 02215.
A Papadopoulos-Sergiou
B Berse
E J Manseau
K Tognazzi
C A Perruzzi
H F Dvorak
D R Senger
Beth Israel Deaconess Hospital · US

Funding

SECRETED PHOSPHOPROTEINS ASSOCIATED WITH TUMORIGENICITYR01CA034025 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI SENGER, DONALD R · 1986 to 1993
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PATHOGENESIS OF TUMOR STROMA GENERATION &WOUND HEALINGR01CA058845 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI DVORAK, HAROLD FISHER · 1993 to 1997
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SECRETED PHOSPHOPROTEINS ASSOCIATED WITH TUMORIGENICITYR23CA034025 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI SENGER, DONALD R · 1985 to 1985
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NCI NIH HHS CA 34025NCI NIH HHS CA 58845
6 · The paper itself

Abstract

Osteopontin (OPN), a secreted adhesive glycoprotein, is significantly overexpressed in a variety of experimental models of malignancy. Moreover, increased levels of OPN have been detected in the blood of patients with metastatic carcinoma. To investigate OPN expression and distribution in human carcinomas directly, we studied a wide variety of common tumors by Northern analysis, in situ hybridization, and immunohistochemistry. All 14 tumors studied by Northern analysis showed very substantial increases in OPN messenger (m)RNA when compared to corresponding normal tissues. Moreover, intense labeling for OPN mRNA was detected in 71 of 76 carcinomas studied by in situ hybridization. In most of the carcinomas studied (colon, stomach, duodenum, pancreas, breast, lung, bladder, prostate, ovary, thyroid, and melanoma), tumor cells did not label detectably for OPN mRNA; however, macrophages intimately associated with tumor cells labeled strongly for the OPN transcript. In carcinomas of the kidney and endometrium, both tumor cells and host macrophages labeled strongly for OPN mRNA. The presence of OPN mRNA in macrophages was particularly pronounced at the edge of tumors (ie, the tumor/stroma interface) and in areas of tumor necrosis. Although in most cases tumor cells did not label detectably for OPN mRNA, both tumor cells and macrophages stained for OPN protein, suggesting that OPN secreted by macrophages may bind to tumor cells, possibly through the glycine-arginine-glycine-aspartate-serine cell binding domain in OPN. Collectively, these data suggest that OPN functions in adhesive interactions at the tumor/host interface and thereby may influence processes such as invasion and metastasis.

Indexed as

Blotting, NorthernBreast NeoplasmsCarcinomaGastrointestinal NeoplasmsHumansImmunohistochemistryIn Situ HybridizationLymphatic MetastasisMacrophagesNeoplasmsOsteopontinRNA, MessengerSialoglycoproteinsOsteopontinRNA, MessengerSialoglycoproteinsSPP1 protein, human

Identifiers

PMID8080043
PMCPMC1890312
OpenAlexW1605025243

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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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.