Evidence map›Paper›PMID 25031014›Full record

ArticleVirchows Archiv : an international journal of pathology2014

Cutaneous carcinosarcoma: further insights into its mutational landscape through massive parallel genome sequencing.

Alberto Paniz-Mondolfi, Rajesh Singh, George Jour, Mandana Mahmoodi, A Hafeez Diwan, Bedia A Barkoh, Ronald Cason, Yve Huttenbach, Gustavo Benaim, John Galbincea and 1 more

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Article in Virchows Archiv : an international journal of pathology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Alberto Paniz-MondolfiDepartment of Pathology and Immunology, Baylor College of Medicine, Houston, TX, USA, albertopaniz@yahoo.com.
Rajesh Singh
George Jour
Mandana Mahmoodi
A Hafeez Diwan
Bedia A Barkoh
Ronald Cason
Yve Huttenbach
Gustavo Benaim
John Galbincea
Rajyalakshmi Luthra

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cutaneous carcinosarcoma (CCS) is an extraordinarily rare neoplasm with a biphasic morphological pattern exhibiting both epithelial and sarcomatoid components. Although its histogenesis and biological aspects remain poorly understood, previous studies have postulated that this tumor may arise from single cancer stem cells which subsequently differentiate into distinct tumor lineages. In this study, we explored a wide array of mutational hot spot regions, through high-depth next-generation sequencing of 47 cancer-associated genes in order to assess the mutational landscape of these tumors and investigate whether the epithelial and mesenchymal components shared the same genetic signatures. Results from this study confirm that despite their striking phenotypic differences, both elements of this infrequent tumor indeed share a common clonal origin. Additionally, CCS appears to embrace a heterogeneous spectrum with specific underlying molecular signatures correlating with the defining epithelial morphotype, with those carcinosarcomas exhibiting a squamous cell carcinoma epithelial component exhibiting diverse point mutations and deletions in the TP53 gene, and those with a basal cell carcinoma morphotype revealing a more complex mutational landscape involving several genes. Also, the fact that our findings involve several targetable gene pathways suggests that the underlying molecular events driving the pathogenesis of CCS may represent future potential targets for personalized therapies.

Indexed as

Genome, HumanMutationAgedAged, 80 and overCarcinosarcomaEpithelial-Mesenchymal TransitionFemaleHumansMaleMiddle AgedSkin Neoplasms

Identifiers

What OpenQuestion holds

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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.