Evidence map›Paper›PMID 27054564›Full record

ArticleHuman vaccines & immunotherapeutics2016

Heparanase and cancer progression: New directions, new promises.

Gil Arvatz, Marina Weissmann, Neta Ilan, Israel Vlodavsky

Open access · bronzeAbstract read
In one paragraph

Article in Human vaccines & immunotherapeutics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
2.7field-weighted citation impact, top 12% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 33 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

4 authors.

Gil Arvatza Cancer and Vascular Biology Research Center, Rappaport Faculty of Medicine, Technion , Haifa , Israel.
Marina Weissmanna Cancer and Vascular Biology Research Center, Rappaport Faculty of Medicine, Technion , Haifa , Israel.
Neta Ilana Cancer and Vascular Biology Research Center, Rappaport Faculty of Medicine, Technion , Haifa , Israel.
Israel Vlodavskya Cancer and Vascular Biology Research Center, Rappaport Faculty of Medicine, Technion , Haifa , Israel.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Heparanase, the sole heparan sulfate degrading endoglycosidase, regulates multiple biological activities that enhance tumor growth, angiogenesis and metastasis. Much of the impact of heparanase on tumor progression is related to its function in mediating tumor-host crosstalk, priming the tumor microenvironment to better support tumor progression. Heparanase expression is enhanced in almost all cancers examined including various carcinomas, sarcomas and hematological malignancies. Numerous clinical association studies have consistently demonstrated that upregulated heparanase expression correlates with increased tumor size, tumor angiogenesis, enhanced metastasis and poor prognosis. Notably, heparanase is ranked among the most frequently recognized tumor antigens in patients with pancreatic, colorectal or breast cancer, favoring heparanase-based immunotherapy. Development of heparanase inhibitors focused on carbohydrate-based compounds of which 4 are being evaluated in clinical trials for various types of cancer, including myeloma, pancreatic carcinoma and hepatocellular carcinoma. Owing to their heparin-like nature, these compounds may exert off target effects. Newly generated heparanase neutralizing monoclonal antibodies profoundly attenuated myeloma and lymphoma tumor growth and dissemination in preclinical models, likely by targeting heparanase in the tumor microenvironment.

Indexed as

CarcinogenesisAnimalsAntineoplastic AgentsClinical Trials as TopicDrug Evaluation, PreclinicalEnzyme InhibitorsGlucuronidaseHeparanaseHumansNeoplasmsAntineoplastic AgentsEnzyme InhibitorsGlucuronidaseHeparanaseHeparanaseimmunotherapylymphomaneutralizing monoclonal antibodytumor microenvironment

Identifiers

PMID27054564
PMCPMC5027699
OpenAlexW2323982843

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.