Evidence map›Paper›PMID 37006233›Full record

ReviewFrontiers in immunology2023

CAXII inhibitors: Potential sensitizers for immune checkpoint inhibitors in HCC treatment.

Rui Han, Jiayin Li, Jing Hony, Zhiwei Xiao, Jinghui Wang, Man Yao, Shufang Liang, Lingeng Lu

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2023. 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
1.1field-weighted citation impact, top 23% 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, 7 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Frontiers in pharmacology · 2024
    Article
  7. Review
  8. Review
  9. Article
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 3 institutions in 2 countries.

Rui HanDepartment of Chinese Medicine Oncology, The First Affiliated Hospital of Naval Medical University, Shanghai, China.
Jiayin LiDepartment of Oncology, The First Hospital Affiliated to Guangzhou University of Chinese Medicine, Guangzhou, China.
Jing HonyDepartment of Chinese Medicine Oncology, The First Affiliated Hospital of Naval Medical University, Shanghai, China.
Zhiwei XiaoDepartment of Oncology, The First Hospital Affiliated to Guangzhou University of Chinese Medicine, Guangzhou, China.
Jinghui WangDepartment of Oncology, The First Hospital Affiliated to Guizhou University of Chinese Medicine, Guiyang, China.
Man YaoDepartment of Chinese Medicine Oncology, The First Affiliated Hospital of Naval Medical University, Shanghai, China.
Shufang LiangDepartment of Chinese Medicine Oncology, The First Affiliated Hospital of Naval Medical University, Shanghai, China.
Lingeng LuDepartment of Chronic Disease Epidemiology, Yale School of Public Health, New Haven, CT, United States.
First Affiliated Hospital of Guangzhou University of Chinese Medicine · CNYale Cancer Center · USGuizhou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is a lethal malignancy with a lack of effective treatments particularly for the disease at an advanced stage. Even though immune checkpoint inhibitors (ICIs) have made great progress in the treatment of HCC, durable and ideal clinical benefits still cannot be achieved in plenty of patients with HCC. Therefore, novel and refined ICI-based combination therapies are still needed to enhance the therapeutic effect. The latest study has reported that the carbonic anhydrase XII inhibitor (CAXIIi), a novel type of anticancer drug, can modify the tumor immunosuppression microenvironment by affecting hypoxic/acidic metabolism and alter the functions of monocytes and macrophages by regulating the expression of C-C motif chemokine ligand 8 (CCL8). These observations shine a light on improving programmed cell death protein 1 (PD-1)/programmed cell death ligand-1 (PD-L1) immunotherapy in combination with CAXIIis. This mini-review aims to ignite enthusiasm to explore the potential application of CAXIIis in combination with immunotherapy for HCC.

Indexed as

Antineoplastic AgentsCarcinoma, HepatocellularLiver NeoplasmsHumansImmune Checkpoint InhibitorsLigandsTumor MicroenvironmentAntineoplastic AgentsImmune Checkpoint InhibitorsLigandsantitumor immunityCAXII inhibitionhepatocellular carcinomaICIs based therapysensitizersynergistic effectTiliroside

Identifiers

PMID37006233
PMCPMC10061011
OpenAlexW4327618220

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.