Evidence map›Paper›PMID 35326544›Full record

ReviewCancers2022

Carbonic Anhydrase IX: A Renewed Target for Cancer Immunotherapy.

Najla Santos Pacheco de Campos, Bruna Santos Souza, Giselle Correia Próspero da Silva, Victoria Alves Porto, Ghanbar Mahmoodi Chalbatani, Gabriela Lagreca, Bassam Janji, Eloah Rabello Suarez

Open access · goldAbstract readReview
In one paragraph

Review in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
3.4field-weighted citation impact, top 6% 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

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 40 citations in OpenAlex.

  1. Pooled it
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  13. Preclinical Characterization of DPI-4452: AJournal of nuclear medicine : official publication, Society of Nuclear Medicine · 2024
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  19. Molecular Imaging Diagnosis of Renal Cancer UsingDiagnostics (Basel, Switzerland) · 2023
    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

8 authors at 2 institutions in 2 countries.

Najla Santos Pacheco de CamposCenter for Natural and Human Sciences, Federal University of ABC, Santo André 09210-580, SP, Brazil.ORCID 0000-0002-2019-5947
Bruna Santos SouzaCenter for Natural and Human Sciences, Federal University of ABC, Santo André 09210-580, SP, Brazil.ORCID 0000-0001-5579-6809
Giselle Correia Próspero da SilvaCenter for Natural and Human Sciences, Federal University of ABC, Santo André 09210-580, SP, Brazil.
Victoria Alves PortoCenter for Natural and Human Sciences, Federal University of ABC, Santo André 09210-580, SP, Brazil.
Ghanbar Mahmoodi ChalbataniTumor Immunotherapy and Microenvironment (TIME) Group, Department of Cancer Research, Luxembourg Institute of Health, 1445 Luxembourg, Luxembourg.ORCID 0000-0003-0738-4708
Gabriela LagrecaCenter for Natural and Human Sciences, Federal University of ABC, Santo André 09210-580, SP, Brazil.ORCID 0000-0001-5438-8512
Bassam JanjiTumor Immunotherapy and Microenvironment (TIME) Group, Department of Cancer Research, Luxembourg Institute of Health, 1445 Luxembourg, Luxembourg.ORCID 0000-0002-9763-0943
Eloah Rabello SuarezCenter for Natural and Human Sciences, Federal University of ABC, Santo André 09210-580, SP, Brazil.ORCID 0000-0002-0521-1056
Universidade Federal do ABC · BRLuxembourg Institute of Health · LU

Funding

Fondation Recherche Cancer et Sang, Luxembourg (INCOM BIOM)Luxembourg National Research Fund (BRIDGES2020/BM/15412275/SMART COMBO)São Paulo Research Foundation 2018/17656-0
6 · The paper itself

Abstract

The carbonic anhydrase isoform IX (CAIX) enzyme is constitutively overexpressed in the vast majority of clear cell renal cell carcinoma (ccRCC) and can also be induced in hypoxic microenvironments, a major hallmark of most solid tumors. CAIX expression is restricted to a few sites in healthy tissues, positioning this molecule as a strategic target for cancer immunotherapy. In this review, we summarized preclinical and clinical data of immunotherapeutic strategies based on monoclonal antibodies (mAbs), fusion proteins, chimeric antigen receptor (CAR) T, and NK cells targeting CAIX against different types of solid malignant tumors, alone or in combination with radionuclides, cytokines, cytotoxic agents, tyrosine kinase inhibitors, or immune checkpoint blockade. Most clinical studies targeting CAIX for immunotherapy were performed using G250 mAb-based antibodies or CAR T cells, developed primarily for bioimaging purposes, with a limited clinical response for ccRCC. Other anti-CAIX mAbs, CAR T, and NK cells developed with therapeutic intent presented herein offered outstanding preclinical results, justifying further exploration in the clinical setting.

Indexed as

antitumor monoclonal antibodiescarbonic anhydrasechimeric antigen receptorclear cell renal cell cancerhypoxic tumorsimmune checkpoint inhibitorsimmunotherapies

Identifiers

PMID35326544
PMCPMC8946730
OpenAlexW4221077414

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.