Evidence map›Paper›PMID 33670942›Full record

ReviewInternational journal of molecular sciences2021

Emerging Immunotherapies against Novel Molecular Targets in Breast Cancer.

Vignesh Sivaganesh, Nazifa Promi, Salma Maher, Bela Peethambaran

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.9field-weighted citation impact, top 11% 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

15 citing papers in PubMed, 25 citations in OpenAlex.

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  13. Protein Tyrosine Phosphatases: Mechanisms in Cancer.International journal of molecular sciences · 2021
    Review
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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 2 institutions in 1 country.

Vignesh SivaganeshDepartment of Biological Sciences, University of the Sciences, 600 S 43rd St, Philadelphia, PA 19104, USA.
Nazifa PromiDepartment of Biological Sciences, University of the Sciences, 600 S 43rd St, Philadelphia, PA 19104, USA.
Salma MaherDepartment of Biological Sciences, University of the Sciences, 600 S 43rd St, Philadelphia, PA 19104, USA.
Bela PeethambaranDepartment of Biological Sciences, University of the Sciences, 600 S 43rd St, Philadelphia, PA 19104, USA.
University of the Sciences · USPhiladelphia College of Osteopathic Medicine · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immunotherapy is a highly emerging form of breast cancer therapy that enables clinicians to target cancers with specific receptor expression profiles. Two popular immunotherapeutic approaches involve chimeric antigen receptor-T cells (CAR-T) and bispecific antibodies (BsAb). Briefly mentioned in this review as well is the mRNA vaccine technology recently popularized by the COVID-19 vaccine. These forms of immunotherapy can highly select for the tumor target of interest to generate specific tumor lysis. Along with improvements in CAR-T, bispecific antibody engineering, and therapeutic administration, much research has been done on novel molecular targets that can especially be useful for triple-negative breast cancer (TNBC) immunotherapy. Combining emerging immunotherapeutics with tumor marker discovery sets the stage for highly targeted immunotherapy to be the future of cancer treatments. This review highlights the principles of CAR-T and BsAb therapy, improvements in CAR and BsAb engineering, and recently identified human breast cancer markers in the context of in vitro or in vivo CAR-T or BsAb treatment.

Indexed as

AnimalsAntibodies, BispecificBiomarkers, TumorBreast NeoplasmsCancer VaccinesCD8-Positive T-LymphocytesCOVID-19COVID-19 VaccinesFemaleHumansImmunotherapyImmunotherapy, AdoptiveMolecular Targeted TherapymRNA VaccinesReceptors, Chimeric AntigenSARS-CoV-2Antibodies, BispecificBiomarkers, TumorCancer VaccinesCOVID-19 VaccinesmRNA VaccinesReceptors, Chimeric AntigenVaccines, Syntheticbispecific antibodiesbreast cancerCAR-Timmune checkpointsimmunotherapymRNA vaccineprecision therapyTNBCtriple-negative breast cancertumor specific/associated antigens

Identifiers

PMID33670942
PMCPMC7957700
OpenAlexW3135268745

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.