Evidence map›Paper›PMID 35882447›Full record

ArticleJournal for immunotherapy of cancer2022

CRISPR-mediated TGFBR2 knockout renders human ovarian cancer tumor-infiltrating lymphocytes resistant to TGF-β signaling.

Samantha M Fix, Marie-Andrée Forget, Donastas Sakellariou-Thompson, Yunfei Wang, Tamara M Griffiths, Minjung Lee, Cara L Haymaker, Ana Lucía Dominguez, Rafet Basar, Christopher Reyes and 5 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03610490 (Clinical Study to Assess Efficacy and Safety of MDA-TIL), which is not on this map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.9field-weighted citation impact, top 5% 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.

NCT03610490 phase2terminatednot on this map

Clinical Study to Assess Efficacy and Safety of MDA-TIL (Autologous Expanded Tumor Infiltrating Lymphocytes) Across Multiple Tumor Types

TypeinterventionalSponsorM.D. Anderson Cancer CenterRan2018 to 2024Enrolled16ConditionsMalignant Solid Neoplasm, Metastatic Colorectal Adenocarcinoma, Metastatic Ovarian Carcinoma, Metastatic Pancreatic Ductal AdenocarcinomaArmsAutologous Tumor Infiltrating Lymphocytes MDA-TIL, Cyclophosphamide, Fludarabine, Interleukin-2, Quality-of-Life Assessment
3 · Its place in the literature

Who cites it

34 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Cellular immunotherapy in melanoma: the next frontier in cancer treatment.Journal of experimental & clinical cancer research : CR · 2026
    Review
  6. Article
  7. Review
  8. Review
  9. Review
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  11. Article
  12. Article
  13. Article
  14. Article
  15. Tumor Microenvironment in Melanoma-Characteristic and Clinical Implications.International journal of molecular sciences · 2025
    Review
  16. Article
  17. Review
  18. Article
  19. Review
  20. 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

15 authors at 2 institutions in 1 country.

Samantha M FixMelanoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.ORCID 0000-0002-1608-4646
Marie-Andrée ForgetMelanoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Donastas Sakellariou-ThompsonMelanoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.ORCID 0000-0001-5954-9557
Yunfei WangMelanoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Tamara M GriffithsBiologics Development, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.ORCID 0000-0002-4597-308X
Minjung LeeTranslational Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.ORCID 0000-0001-5499-044X
Cara L HaymakerTranslational Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.ORCID 0000-0002-1317-9287
Ana Lucía DominguezMelanoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Rafet BasarStem Cell Transplantation and Cellular Therapy, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Christopher ReyesCell Biology R&D, Thermo Fisher Scientific, Carlsbad, California, USA.
Sanjay KumarCell Biology R&D, Thermo Fisher Scientific, Carlsbad, California, USA.
Larissa A MeyerGynecologic Oncology and Reproductive Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.ORCID 0000-0002-2687-7463
Patrick Hwu *Melanoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA Patrick.Hwu@moffitt.org.ORCID 0000-0002-8293-1313
Chantale Bernatchez *Melanoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.ORCID 0000-0001-5926-3460
Amir A Jazaeri *Gynecologic Oncology and Reproductive Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
The University of Texas MD Anderson Cancer Center · USThermo Fisher Scientific (United States) · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Fabien Delerue · 1985 to 2026
$290.8M
NRSA Training CoreTL1TR003169 · NCATS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI CHANDRA, JOYA, FROST, JEFFREY A. · 2019 to 2023
$3.7M
Health Services Career Development: Improving Medical Decisions in Ovarian CancerK07CA201013 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI MEYER, LARISSA ALEJANDRA · 2016 to 2020
$853k
Genetically engineering T cells to overcome the immunosuppressive melanoma microenvironmentF32CA253968 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI FIX, SAMANTHA MARIE · 2020 to 2021
$82k
NCATS NIH HHS TL1 TR003169NCI NIH HHS F32 CA253968NCI NIH HHS K07 CA201013NCI NIH HHS P30 CA016672
6 · The paper itself

Abstract

backgroundThe correlation between elevated T-cell infiltration and improved survival of ovarian cancer (OvCa) patients suggests that endogenous tumor-infiltrating lymphocytes (TIL) possess some degree of antitumor activity that can be harnessed for OvCa immunotherapy. We previously optimized a protocol for ex vivo OvCa TIL expansion for adoptive cell therapy, which is now being tested in a clinical trial at our institution (NCT03610490). Building on this success, we embarked on genetic modification of OvCa TIL to overcome key immunosuppressive factors present in the tumor microenvironment. Here, we present the preclinical optimization of CRISPR/Cas9-mediated knockout of the TGF-β receptor 2 (

methodsOvCa TILs were generated from four patients' tumor samples obtained at surgical resection and subjected to CRISPR/Cas9-mediated knockout of

results

conclusionsCRISPR/Cas9-mediated gene knockout is feasible and efficient in patient-derived OvCa TIL using clinically-scalable methods. We achieved efficient and specific

Indexed as

Lymphocytes, Tumor-InfiltratingOvarian NeoplasmsCarcinoma, Ovarian EpithelialFemaleHumansImmunotherapy, AdoptiveReceptor, Transforming Growth Factor-beta Type IITransforming Growth Factor betaTumor MicroenvironmentReceptor, Transforming Growth Factor-beta Type IITransforming Growth Factor betaCell EngineeringImmunotherapy, AdoptiveLymphocytes, Tumor-Infiltrating

Identifiers

PMID35882447
PMCPMC9330322
OpenAlexW4288047160

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

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.