Evidence map›Paper›PMID 26895102›Full record

ArticleOncotarget2016

The cancer-testis antigens SPANX-A/C/D and CTAG2 promote breast cancer invasion.

Erin A Maine, Jill M Westcott, Amanda M Prechtl, Tuyen T Dang, Angelique W Whitehurst, Gray W Pearson

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

33 citing papers in PubMed, 60 citations in OpenAlex.

  1. Article
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  6. Chronic IL-1 Exposed ARJournal of cellular signaling · 2021
    Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. miR614 Expression Enhances Breast Cancer Cell Motility.International journal of molecular sciences · 2020
    Article
  12. Article
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  16. Review
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  19. PeerJ · 2020
    Article
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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

6 authors at 1 institution in 1 country.

Erin A MaineHarold C. Simmons Cancer Center, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Jill M WestcottHarold C. Simmons Cancer Center, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Amanda M PrechtlHarold C. Simmons Cancer Center, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Tuyen T DangHarold C. Simmons Cancer Center, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Angelique W WhitehurstHarold C. Simmons Cancer Center, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Gray W PearsonHarold C. Simmons Cancer Center, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
The University of Texas Southwestern Medical Center · US

Funding

UT Southwestern Medical Center Simmons Comprehensive Cancer CenterP30CA142543 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI Sandi Leigh Pruitt · 2010 to 2026
$53.7M
Cancer Biology Training GrantT32CA124334 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI SHAY, JERRY WILLIAM · 2007 to 2021
$5.3M
Investigating Breast Cancer Collective InvasionR01CA155241 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI PEARSON, GRAY W · 2011 to 2015
$1.6M
Mechanistic Elaboration of Fragility in the Cancer Cell Mitotic SpindleR01CA154699 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI WHITEHURST, ANGELIQUE WRIGHT · 2011 to 2015
$1.5M
NCI NIH HHS P30 CA142543NCI NIH HHS R01 CA154699NCI NIH HHS R01 CA155241NCI NIH HHS T32 CA124334
6 · The paper itself

Abstract

Genes that are normally biased towards expression in the testis are often induced in tumor cells. These gametogenic genes, known as cancer-testis antigens (CTAs), have been extenstively investigated as targets for immunotherapy. However, despite their frequent detection, the degree to which CTAs support neoplastic invasion is poorly understood. Here, we find that the CTA genes SPANX-A/C/D and CTAG2 are coordinately induced in breast cancer cells and regulate distinct features of invasive behavior. Our functional analysis revealed that CTAG2 interacts with Pericentrin at the centrosome and is necessary for directional migration. Conversely, SPANX-A/C/D interacts with Lamin A/C at the inner nuclear membrane and is required for the formation of actin-rich cellular protrusions that reorganize the extracellular matrix. Importantly, SPANX-A/C/D was required for breast cancer cells to spontaneously metastasize to the lung, demonstrating that CTA reactivation can be critical for invasion dependent phenotypes in vivo. Moreover, elevated SPANX-A/C/D expression in breast cancer patient tumors correlated with poor outcome. Together, our results suggest that distinct CTAs promote tumor progression by regulating complementary cellular functions that are integrated together to induce invasive behavior.

Indexed as

AnimalsAntigens, NeoplasmAntigens, SurfaceApoptosisBiomarkers, TumorBreast NeoplasmsCell MovementCell ProliferationFemaleHumansMiceMice, Inbred NODMice, SCIDNeoplasm InvasivenessNeoplasm ProteinsNeoplasm StagingAntigens, NeoplasmAntigens, SurfaceBiomarkers, TumorCTAG2 protein, humanNeoplasm ProteinsNuclear ProteinsSPANXA1 protein, humanSPANXC protein, humanSPANXD protein, humanbreast cancercancer-testis antigenextracellular matrixinvasionmetastasis

Identifiers

PMID26895102
PMCPMC4924746
OpenAlexW2281019288

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.