Evidence map›Paper›PMID 32671955›Full record

ReviewCancer reports (Hoboken, N.J.)2020

Altered mitochondrial trafficking as a novel mechanism of cancer metastasis.

Madison Furnish, M Cecilia Caino

Open access · greenAbstract readReview
In one paragraph

Review in Cancer reports (Hoboken, N.J.), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

21 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
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  6. Article
  7. Review
  8. Review
  9. Article
  10. Loss of the fructose transporter SLC2A5 inhibits cancer cell migration.Frontiers in cell and developmental biology · 2022
    Article
  11. Mitochondrial Fission and Fusion in Tumor Progression to Metastasis.Frontiers in cell and developmental biology · 2022
    Review
  12. Miro proteins and their role in mitochondrial transfer in cancer and beyond.Frontiers in cell and developmental biology · 2022
    Review
  13. Review
  14. Review
  15. Review
  16. Review
  17. Article
  18. Mitochondria Targeting as an Effective Strategy for Cancer Therapy.International journal of molecular sciences · 2020
    Review
  19. Review
  20. Intracellular Transport in Cancer Metabolic Reprogramming.Frontiers in cell and developmental biology · 2020
    Review
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.

Madison FurnishDepartment of Pharmacology, University of Colorado School of Medicine, Aurora, Colorado, USA.ORCID 0000-0002-8483-5579
M Cecilia CainoDepartment of Pharmacology, University of Colorado School of Medicine, Aurora, Colorado, USA.ORCID 0000-0001-8294-8070
University of Colorado Denver · US

Funding

PREDOCTORAL TRAINING PROGRAM IN PHARMACOLOGYT32GM007635 · NIGMS · UNIVERSITY OF COLORADO DENVER · PI DELL'ACQUA, MARK L · 1985 to 2023
$6.1M
Mitochondrial Hsp90s Regulation of Tumor Bioenergetics and MetastasisF32CA177018 · NCI · WISTAR INSTITUTE · PI CAINO, MARIA CECILIA · 2013 to 2015
$171k
NCI NIH HHS F32 CA177018NIGMS NIH HHS T32 GM007635
6 · The paper itself

Abstract

backgroundMammalian cells must constantly reprogram the distribution of mitochondria in order to meet the local demands for energy, calcium, redox balance, and other mitochondrial functions. Mitochondrial localization inside the cell is a result of a combination of movement along the microtubule tracks plus anchoring to actin filaments. RECENT

findingsRecent advances show that subcellular distribution of mitochondria can regulate tumor cell growth, proliferation/motility plasticity, metastatic competence, and therapy responses in tumors. In this review, we discuss our current understanding of the mechanisms by which mitochondrial subcellular distribution is regulated in tumor cells.

conclusionsMitochondrial trafficking is dysregulated in tumors. Accumulation of mitochondria at the leading edge of the cell supports energy expensive processes of focal adhesion dynamics, cell membrane dynamics, migration, and invasion.

Indexed as

Neoplasm MetastasisAdenosine TriphosphateAnimalsCell MovementFocal AdhesionsHumansMembrane ProteinsMicrotubulesMitochondriaMyosin Heavy ChainsMyosinsMyosin Type VNeoplasm InvasivenessNerve Tissue ProteinsSignal TransductionAdenosine TriphosphateMembrane ProteinsMyo19 protein, humanMYO5A protein, humanMyosin Heavy ChainsMyosinsMyosin Type VNerve Tissue ProteinsSNPH protein, humancancerdyneinkinesinmitochondriamyosintrafficking

Identifiers

PMID32671955
PMCPMC7370516
OpenAlexW2911357126

What OpenQuestion holds

Textmetadata
LicenceTDM
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.