Evidence map›Paper›PMID 32858103›Full record

ReviewCancer letters2020

Therapy-induced chemoexosomes: Sinister small extracellular vesicles that support tumor survival and progression.

Shyam K Bandari, Kaushlendra Tripathi, Sunil Rangarajan, Ralph D Sanderson

Open access · greenAbstract readReview
In one paragraph

Review in Cancer letters, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.5field-weighted citation impact, top 37% 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

9 citing papers in PubMed, 12 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

4 authors at 1 institution in 1 country.

Shyam K BandariDepartment of Pathology, O'Neal Comprehensive Cancer Center, 1824 6th Avenue South, Wallace Tumor Institute, Room 603, University of Alabama at Birmingham, Birmingham, AL, 35294, USA. Electronic address: skbandari@uabmc.edu.
Kaushlendra TripathiDepartment of Pathology, O'Neal Comprehensive Cancer Center, 1824 6th Avenue South, Wallace Tumor Institute, Room 603, University of Alabama at Birmingham, Birmingham, AL, 35294, USA.
Sunil RangarajanDepartment of Pathology, O'Neal Comprehensive Cancer Center, 1824 6th Avenue South, Wallace Tumor Institute, Room 603, University of Alabama at Birmingham, Birmingham, AL, 35294, USA.
Ralph D SandersonDepartment of Pathology, O'Neal Comprehensive Cancer Center, 1824 6th Avenue South, Wallace Tumor Institute, Room 603, University of Alabama at Birmingham, Birmingham, AL, 35294, USA. Electronic address: ralphsanderson@uabmc.edu.
University of Alabama at Birmingham · US

Funding

Heparanase Regulation of Myeloma Metastasis: Mechanism and TherapyR01CA138340 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI SANDERSON, RALPH D · 2009 to 2018
$3.3M
Heparanase in Tumor Progression, Metastasis and ChemoresistanceR01CA211752 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI SANDERSON, RALPH D · 2017 to 2021
$1.7M
NCI NIH HHS R01 CA138340NCI NIH HHS R01 CA211752
6 · The paper itself

Abstract

Chemotherapy involves the use of multiple cytotoxic or cytostatic drugs acting by various mechanisms to kill or arrest the growth of cancer cells. Chemotherapy remains the most utilized approach for controlling cancer. Emerging evidence indicates that cancer cells activate various pro-survival mechanisms to cope with chemotherapeutic stress. These mechanisms persist during treatment and often help orchestrate tumor regrowth and patient relapse. Exosomes due to their nature of carrying and transferring multiple biologically active components have emerged as key players in cancer pathogenesis. Recent data demonstrates that chemotherapeutic stress enhances the secretion and alters the cargo carried by exosomes. These altered exosomes, which we refer to as chemoexosomes, are capable of transferring cargo to target tumor cells that can enhance their chemoresistance, increase their metastatic behavior and in certain cases even aid in endowing tumor cells with cancer stem cell-like properties. This mini-review summarizes the recent developments in our understanding of the impact chemoexosomes have on tumor survival and progression.

Indexed as

Drug Resistance, NeoplasmAntineoplastic AgentsExosomesGene Expression Regulation, NeoplasticHumansNeoplasmsNeoplastic Stem CellsAntineoplastic AgentsChemoresistanceChemotherapyExosomesMetastasisStemness

Identifiers

PMID32858103
PMCPMC7685072
OpenAlexW3081047538

What OpenQuestion holds

Textmetadata
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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.