Evidence map›Paper›PMID 27669439›Full record

ArticleOncogene2017

The MACC1-SPON2 axis: a new biomarker and therapeutic target in colorectal cancer.

P Chandrasinghe, J Stebbing, J Warusavitarne

Abstract readLetterComment
PubMed Publisher
In one paragraph

Article in Oncogene, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
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

9 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

P ChandrasingheDepartment of Surgery, St. Mark's Hospital and Imperial College, London, UK.
J StebbingImperial College, Hammersmith Hospital, London, UK.
J WarusavitarneDepartment of Surgery, St. Mark's Hospital and Imperial College, London, UK.

Funding

Department of Health NIHR-RP-011-053
6 · The paper itself

Abstract

In this issue of the Journal, Schmid et al identify Spondin 2 (SPON2) as a prominent downstream signaling target of metastasis-associated in colon cancer 1 (MACC1) in colorectal cancer (CRC). It is shown that SPON2 mediates MACC1-induced CRC cell proliferation, invasion and metastasis in vitro and in vivo, while its high expression correlates with adverse disease free survival in clinical samples. Therefore, not only does this study shed further light into the complexity of colorectal carcinogenesis, but it also puts forward a potential novel prognostic biomarker to predict high-risk tumors before they metastasize. The MACC1/SPON2 axis may also have utility beyond an indicator of tumor aggressiveness and lends itself as a promising therapeutic target for colorectal and potentially other solid tumors.

Indexed as

Gene Expression Regulation, NeoplasticBiomarkers, TumorCell Transformation, NeoplasticColorectal NeoplasmsExtracellular Matrix ProteinsHumansNeoplasm ProteinsSignal TransductionTrans-ActivatorsTranscription FactorsBiomarkers, TumorExtracellular Matrix ProteinsMACC1 protein, humanNeoplasm ProteinsSPON2 protein, humanTrans-ActivatorsTranscription Factors

Identifiers

PMID27669439

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.