Evidence map›Paper›PMID 30261276›Full record

ReviewSeminars in cancer biology2018

The role of cancer stem cells in the modulation of anti-tumor immune responses.

Cristina Maccalli, Kakil Ibrahim Rasul, Mamoun Elawad, Soldano Ferrone

Open access · greenAbstract readReview
In one paragraph

Review in Seminars in cancer biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
4.6field-weighted citation impact, top 3% 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

63 citing papers in PubMed, 101 citations in OpenAlex.

  1. Article
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  12. The role of HSP40 in cancer: Recent advances.Histology and histopathology · 2024
    Review
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3 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

4 authors at 3 institutions in 2 countries.

Cristina MaccalliClinical Research Center, Translational Medicine, Sidra Medicine, Doha, Qatar. Electronic address: cmaccalli@sidra.org.
Kakil Ibrahim RasulHaemtology and Oncology Department, National Center for Cancer Care and Research (NCCCR), Hamad Medical Corporation, Doha, Qatar.
Mamoun ElawadGastroenterology, Hepatology and Nutrition Department, Sidra Medicine, Doha, Qatar.
Soldano FerroneDepartment of Surgery, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
Harvard University · USNational Center for Cancer Care and Research · QAQatar Airways (Qatar) · QA

Funding

T cell plasticity, fusion proteins and CAR T cell-based immunotherapy of head and neck cancerR01DE028172 · NIDCR · MASSACHUSETTS GENERAL HOSPITAL · PI WANG, XINHUI · 2018 to 2022
$1.9M
IL-15 TRiKES-based specific immunotherapy of pancreatic ductal adenocarcinomaR03CA231766 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI FERRONE, CRISTINA R., FERRONE, SOLDANO · 2018 to 2019
$177k
IL-15 TRiKES-based specific immunotherapy of TNBC; resistance mechanismsR03CA216114 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI FERRONE, SOLDANO, VALLERA, DANIEL A · 2018 to 2019
$177k
Safety and anti-tumor activity of B7-H3 CAR T cells in TNBCR03CA223886 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI DOTTI, GIANPIETRO, FERRONE, SOLDANO · 2018 to 2019
$176k
NCI NIH HHS R03 CA216114NCI NIH HHS R03 CA223886NCI NIH HHS R03 CA231766NIDCR NIH HHS R01 DE028172
6 · The paper itself

Abstract

Tumor lesions comprise multiple subpopulations of cells including those endowed with "stemness" properties. The latter cells are responsible of tumor initiation, metastasis formation, resistance to conventional therapies and disease recurrence. These relatively rare cells denominated cancer stem cells (CSCs) or cancer initiating cells (CICs) are defined based on self-renewing, multipotency and tumorigenicity. These cells through their immunomodulating features can evade from immunesurveillance, persisting in the form of quiescence and dormancy. They can drive the neoplastic growth and recurrence, even after long latency. Moreover, CSCs/CICs due to their ability to modulate and shape immune responses can represent the component of a tumor causing immunotherapy resistance in cancer patients. In this review a general overview of immunological properties of CSCs/CICs is provided, with a special focus on the mechanisms of modulation of T cell mediated responses. The need to further dissect the mechanisms regulating the immunological profile of CSCs/CICs and their interactions with immune cells and tumor microenvironment is discussed. An improved characterization of the immunological properties of CSCs/CICs will contribute to the rationale design of immunotherapeutic interventions which target these cells and may lead to the eradication of malignant diseases.

Indexed as

AnimalsGene Expression Regulation, NeoplasticHumansImmunologic SurveillanceImmunotherapyMicroRNAsNeoplasmsNeoplastic Stem CellsT-LymphocytesTumor MicroenvironmentMicroRNAsCancer stem cellsImmune-based interventionsImmune escape mechanismsImmunological profilingTumor dormancy

Identifiers

PMID30261276
PMCPMC8668198
OpenAlexW2892469487

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.