Evidence map›Paper›PMID 35328459›Full record

ReviewInternational journal of molecular sciences2022

Exploiting Radiation Induction of Antigens in Cancer: Targeted Drug Delivery.

Vaishali Kapoor, Abhay K Singh, Calvin D Lewis, Sapna Deore, Dennis E Hallahan

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.6field-weighted citation impact, top 36% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Complement system in cancer: friend or foe of immunotherapy.Journal for immunotherapy of cancer · 2026
    Review
  2. Proton radiation boosts the efficacy of mesothelin-targeting chimeric antigen receptor T cell therapy in pancreatic cancer.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  3. Development of a [89Zr]Zr-labeled Human Antibody using a Novel Phage-displayed Human scFv Library.Clinical cancer research : an official journal of the American Association for Cancer Research · 2024
    Article
  4. Blocking the functional domain of TIP1 by antibodies sensitizes cancer to radiation therapy.Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie · 2023
    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

5 authors at 2 institutions in 1 country.

Vaishali KapoorDepartment of Radiation Oncology, Washington University School of Medicine in St. Louis, St. Louis, MO 63108, USA.ORCID 0000-0002-7581-1487
Abhay K SinghDepartment of Radiation Oncology, Washington University School of Medicine in St. Louis, St. Louis, MO 63108, USA.ORCID 0000-0001-8399-7974
Calvin D LewisDepartment of Radiation Oncology, Washington University School of Medicine in St. Louis, St. Louis, MO 63108, USA.ORCID 0000-0003-2673-5884
Sapna DeoreMedical Guidance Systems LLC, St. Louis, MO 63110, USA.
Dennis E HallahanDepartment of Radiation Oncology, Washington University School of Medicine in St. Louis, St. Louis, MO 63108, USA.
Washington University in St. Louis · USUniversity of Iowa · US

Funding

ROLE OF MIDKINE IN MOLECULAR TARGETED THERAPY TO TIP1 FOR LUNG CANCER TREATMENTK22CA234404 · NCI · WASHINGTON UNIVERSITY · PI KAPOOR, VAISHALI · 2020 to 2022
$460k
Elsa U. Pardee Foundation K22CA234404National Institute of Health R41CA233020National Institute of Health R44CA210687NCI NIH HHS K22 CA234404
6 · The paper itself

Abstract

Therapeutic antibodies used to treat cancer are effective in patients with advanced-stage disease. For example, antibodies that activate T-lymphocytes improve survival in many cancer subtypes. In addition, antibody-drug conjugates effectively target cytotoxic agents that are specific to cancer. This review discusses radiation-inducible antigens, which are stress-regulated proteins that are over-expressed in cancer. These inducible cell surface proteins become accessible to antibody binding during the cellular response to genotoxic stress. The lead antigens are induced in all histologic subtypes and nearly all advanced-stage cancers, but show little to no expression in normal tissues. Inducible antigens are exploited by using therapeutic antibodies that bind specifically to these stress-regulated proteins. Antibodies that bind to the inducible antigens GRP78 and TIP1 enhance the efficacy of radiotherapy in preclinical cancer models. The conjugation of cytotoxic drugs to the antibodies further improves cancer response. This review focuses on the use of radiotherapy to control the cancer-specific binding of therapeutic antibodies and antibody-drug conjugates.

Indexed as

Antineoplastic AgentsImmunoconjugatesNeoplasmsDrug Delivery SystemsHumansAntineoplastic AgentsImmunoconjugatesantibody–drug conjugateradiation-inducibleradiation therapytherapeutic target

Identifiers

PMID35328459
PMCPMC8953554
OpenAlexW4220933838

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.