Evidence map›Paper›PMID 32752017›Full record

ReviewInternational journal of molecular sciences2020

Crosstalk between Tumor and Stromal Cells in Pancreatic Ductal Adenocarcinoma.

Nadine Sperb, Miltiadis Tsesmelis, Thomas Wirth

Abstract 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 70 papers.

0numbers the graph read from it
0cells of the map it votes in
70citing 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

70 citing papers in PubMed.

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10 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

3 authors.

Nadine SperbInstitute of Physiological Chemistry, University of Ulm, 89081 Ulm, Germany.
Miltiadis TsesmelisInstitute of Physiological Chemistry, University of Ulm, 89081 Ulm, Germany.ORCID 0000-0002-7438-580X
Thomas WirthInstitute of Physiological Chemistry, University of Ulm, 89081 Ulm, Germany.

Funding

Deutsche Forschungsgemeinschaft GRK 2254, project number 288342734
6 · The paper itself

Abstract

Pancreatic ductal adenocarcinoma (PDAC) remains a lethal cancer. The poor prognosis calls for a more detailed understanding of disease biology in order to pave the way for the development of effective therapies. Typically, the pancreatic tumor is composed of a minority of malignant cells within an excessive tumor microenvironment (TME) consisting of extracellular matrix (ECM), fibroblasts, immune cells, and endothelial cells. Research conducted in recent years has particularly focused on cancer-associated fibroblasts (CAFs) which represent the most prominent cellular component of the desmoplastic stroma. Here, we review the complex crosstalk between CAFs, tumor cells, and other components of the TME, and illustrate how these interactions drive disease progression. We also discuss the emerging field of CAF heterogeneity, their tumor-supportive versus tumor-suppressive capacity, and the consequences for designing stroma-targeted therapies in the future.

Indexed as

Tumor MicroenvironmentCancer-Associated FibroblastsCarcinoma, Pancreatic DuctalCell CommunicationHumansPancreatic NeoplasmsStromal CellsCAFCAF heterogeneitycancer metabolismimmune microenvironmentPDACtumor microenvironment

Identifiers

PMID32752017
PMCPMC7432853

What OpenQuestion holds

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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.