Evidence map›Paper›PMID 33105836›Full record

ReviewInternational journal of molecular sciences2020

Wnt-Independent and Wnt-Dependent Effects of APC Loss on the Chemotherapeutic Response.

Casey D Stefanski, Jenifer R Prosperi

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
4.0field-weighted citation impact, top 5% 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

25 citing papers in PubMed, 52 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

2 authors at 1 institution in 1 country.

Casey D StefanskiDepartment of Biological Sciences, University of Notre Dame, Notre Dame, IN 46617, USA.
Jenifer R ProsperiDepartment of Biological Sciences, University of Notre Dame, Notre Dame, IN 46617, USA.ORCID 0000-0001-8439-4411
University of Notre Dame · US

Funding

American Cancer Society RSG-TBG-133116
6 · The paper itself

Abstract

Resistance to chemotherapy occurs through mechanisms within the epithelial tumor cells or through interactions with components of the tumor microenvironment (TME). Chemoresistance and the development of recurrent tumors are two of the leading factors of cancer-related deaths. The Adenomatous Polyposis Coli (APC) tumor suppressor is lost in many different cancers, including colorectal, breast, and prostate cancer, and its loss correlates with a decreased overall survival in cancer patients. While APC is commonly known for its role as a negative regulator of the WNT pathway, APC has numerous binding partners and functional roles. Through APC's interactions with DNA repair proteins, DNA replication proteins, tubulin, and other components, recent evidence has shown that APC regulates the chemotherapy response in cancer cells. In this review article, we provide an overview of some of the cellular processes in which APC participates and how they impact chemoresistance through both epithelial- and TME-derived mechanisms.

Indexed as

Adenomatous Polyposis ColiAdenomatous Polyposis Coli ProteinAnimalsColorectal NeoplasmsDrug Resistance, NeoplasmGenes, Tumor SuppressorHumansTumor MicroenvironmentWnt Signaling PathwayAdenomatous Polyposis Coli ProteinAPC protein, humanadenomatous polyposis colichemoresistanceWNT signaling

Identifiers

PMID33105836
PMCPMC7660076
OpenAlexW3093630507

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.