Evidence map›Paper›PMID 37622107›Full record

ArticleFrontiers in immunology2023

Identification of a novel combination treatment strategy in clear cell renal cell carcinoma stem cells with shikonin and ipilimumab.

Chen Lyu, Birgit Stadlbauer, Lili Wang, Alexander Buchner, Heike Pohla

Open access · goldAbstract read
In one paragraph

Article 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 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.8field-weighted citation impact, top 13% 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

8 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. The metastasis landscape ofFrontiers in immunology · 2026
    Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Cancer Stem Cells from Definition to Detection and Targeted Drugs.International journal of molecular sciences · 2024
    Review
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

5 authors at 2 institutions in 2 countries.

Chen LyuTumor Immunology Laboratory, LIFE Center, LMU Klinikum, University Munich, Planegg, Germany.
Birgit StadlbauerTumor Immunology Laboratory, LIFE Center, LMU Klinikum, University Munich, Planegg, Germany.
Lili WangTumor Immunology Laboratory, LIFE Center, LMU Klinikum, University Munich, Planegg, Germany.
Alexander BuchnerTumor Immunology Laboratory, LIFE Center, LMU Klinikum, University Munich, Planegg, Germany.
Heike PohlaTumor Immunology Laboratory, LIFE Center, LMU Klinikum, University Munich, Planegg, Germany.
LMU Klinikum · DELudwig-Maximilians-Universität München · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Management of clear cell renal cell carcinoma (ccRCC) has changed rapidly in recent years with the advent of immune checkpoint inhibitors (ICIs). However, only a limited number of patients can sustainably respond to immune checkpoint inhibitors and many patients develop resistance to therapy, creating an additional need for therapeutic strategies to improve the efficacy of systemic therapies. Methods: Binding probability and target genes prediction using online databases, invasion, migration, and apoptosis assays as well as the inhibition of cancer stem cells (CSCs) markers in ccRCC cell lines were used to select the most promising phytochemicals (PTCs). Mixed lymphocyte tumor cell culture (MLTC) system and flow cytometry were performed to confirm the potential combination strategy. The potential immunotherapeutic targets and novel CSC markers were identified via the NanoString analysis. The mRNA and protein expression, immune signatures as well as survival characteristics of the marker in ccRCC were analyzed via bioinformation analysis. Results: Shikonin was selected as the most promising beneficial combination partner among 11 PTCs for ipilimumab for the treatment of ccRCC patients due to its strong inhibitory effect on CSCs, the significant reduction of FoxP3 Conclusion: We propose that a combination of shikonin and ipilimumab could be a promising treatment strategy and VCAM1 a novel immunotherapeutic target for the treatment of ccRCC.

Indexed as

CarcinomaCarcinoma, Renal CellKidney NeoplasmsHumansImmune Checkpoint InhibitorsIpilimumabLeukocytes, MononuclearNaphthoquinonesNeoplastic Stem CellsImmune Checkpoint InhibitorsIpilimumabNaphthoquinonesshikonincancer stem cells (CSCs)immune checkpoint inhibitor (ICI)immunotherapyphytochemicalrenal cell carcinomatumor infiltrating immune cell (TIC)tumor microenvironment (TME)

Identifiers

PMID37622107
PMCPMC10445237
OpenAlexW4385700793

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.