Evidence map›Paper›PMID 42446663›Full record

ReviewClinical cancer research : an official journal of the American Association for Cancer Research2026

Sex Steroid Hormone Regulation of T-Cell Function and Antitumor Immunity.

Amanda Heard, Rachel T Huynh, Christy R Hagan, Amy E Moran

Abstract readReview
In one paragraph

Review in Clinical cancer research : an official journal of the American Association for Cancer Research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Amanda Heard *Department of Cancer Biology, University of Kansas Medical Center, Kansas City, Kansas.ORCID 0000-0002-7150-7998
Rachel T Huynh *Department of Cell, Developmental and Cancer Biology, Knight Cancer Institute, Oregon Health & Science University, Portland, Oregon.ORCID 0000-0003-4463-5262
Christy R HaganDepartment of Cancer Biology, University of Kansas Medical Center, Kansas City, Kansas.ORCID 0000-0003-2524-1815
Amy E MoranDepartment of Cell, Developmental and Cancer Biology, Knight Cancer Institute, Oregon Health & Science University, Portland, Oregon.ORCID 0000-0003-1952-7737

Funding

Transgenic & Gene-Targeting Shared ResourceP30CA168524 · NCI · UNIVERSITY OF KANSAS MEDICAL CENTER · PI ROY A. JENSEN · 2012 to 2026
$40.1M
The molecular mechanisms of progestin efficacy and resistance in EC-AEHP01CA278735 · NCI · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI Jason Gertz, Kimberly K. Leslie · 2025 to 2026
$7.8M
Understanding how T cell intrinsic androgen receptor activity influences cell differentiation and dysfunctionR37CA263592 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI Amy E Moran · 2021 to 2026
$3.2M
Defining the Mechanistic Basis of Bacterial Androgen Production in Dampening Anti-Tumor Immunity and Promoting Resistance to Androgen Receptor Axis-Targeted Therapies for Metastatic Prostate CancerR01CA287126 · NCI · JOHNS HOPKINS UNIVERSITY · PI Amy E Moran, Jason Michael Ridlon · 2024 to 2026
$1.9M
Targeting the Progesterone Receptor as a Novel Means to Increase Efficacy of Immune Checkpoint Inhibitors in Hormone Receptor Positive Breast CancerR21CA274044 · NCI · UNIVERSITY OF KANSAS MEDICAL CENTER · PI HAGAN, CHRISTY, HARTMAN, ZACHARY CONRAD · 2022 to 2023
$472k
American Cancer Society (ACS) RSG-23-1152337-01-IBCDKuni Foundation (The Kuni Foundation)Mark Foundation For Cancer Research (MFCR)National Cancer Institute (NCI) NCI P01CA278735National Cancer Institute (NCI) P30 CA168524National Cancer Institute (NCI) P50CA097163National Cancer Institute (NCI) R01CA287126National Cancer Institute (NCI) R21CA274044National Cancer Institute (NCI) R37 CA263592NCI NIH HHS P01 CA278735NCI NIH HHS P30 CA168524NCI NIH HHS R01 CA287126NCI NIH HHS R21 CA274044NCI NIH HHS R37 CA263592Polycystic Kidney Disease Charity (PKD Charity) 1195884Prostate Cancer Foundation (PCF) 2023-YIUniversity of Kansas Medical Center (KUMC)U.S. Department of Defense (DOD) BC201209 W81XWH-21-1-0349U.S. Department of Defense (DOD) CA220729P1 HT9425-23-1-0744
6 · The paper itself

Abstract

Cancer immunotherapy treatment has revolutionized cancer care. Of the many FDA-approved immunotherapies, immune checkpoint inhibitors are the most widely prescribed, given their utility in treating both solid and hematopoietic diseases and primary and metastatic malignancies. These therapies are dependent on co-opting the body's natural immunity, and thus conditions affecting the immune system can also determine therapeutic outcomes for patients with cancer. In this review, we examine one such naturally occurring immunomodulatory system: sex steroid hormones. Already thought to play a role in differing outcomes in infectious disease and transplant, sex steroid hormones may be contributing factors to differences in cancer occurrence and immunotherapy success between sexes. We will explore effects of steroid hormones on immune cells, specifically T cells, and the mechanisms through which they exert those effects as reported in the current literature. Androgens and progesterone are reported to exert largely immunosuppressive effects on T cells by promoting differentiation and expansion of immunosuppressive T-cell subpopulations. Interestingly, estrogen has been reported to have both immune-activating and immune-suppressing effects, both of which have the potential to affect the efficacy of immunotherapeutics. Therefore, patient hormonal status should be considered when prescribing immunotherapy for patients with cancer.

Indexed as

Gonadal Steroid HormonesNeoplasmsT-LymphocytesAnimalsFemaleHumansImmunotherapyGonadal Steroid Hormones

Identifiers

PMID42446663
PMCPMC13372207

What OpenQuestion holds

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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.