Evidence map›Paper›PMID 32220968›Full record

ArticleMolecular cancer therapeutics2020

Vitamin D Receptor Activation and Photodynamic Priming Enables Durable Low-dose Chemotherapy.

Sriram Anbil, Michael Pigula, Huang-Chiao Huang, Srivalleesha Mallidi, Mans Broekgaarden, Yan Baglo, Pushpamali De Silva, Diane M Simeone, Mari Mino-Kenudson, Edward V Maytin and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cancer therapeutics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
2.6field-weighted citation impact, top 9% 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

39 citing papers in PubMed, 47 citations in OpenAlex.

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  20. Critical PDT theory II: Current concepts and indications.Photodiagnosis and photodynamic therapy · 2022
    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

12 authors at 4 institutions in 1 country.

Sriram Anbil *Long School of Medicine, UT Health San Antonio, San Antonio, Texas.
Michael Pigula *Wellman Center for Photomedicine, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.ORCID 0000-0001-6121-9995
Huang-Chiao HuangWellman Center for Photomedicine, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.ORCID 0000-0002-5406-0733
Srivalleesha MallidiWellman Center for Photomedicine, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.
Mans BroekgaardenWellman Center for Photomedicine, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.
Yan BagloWellman Center for Photomedicine, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.ORCID 0000-0003-4204-4928
Pushpamali De SilvaWellman Center for Photomedicine, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.
Diane M SimeoneDepartment of Surgery, Langone School of Medicine, New York University, New York, New York.
Mari Mino-KenudsonDepartment of Pathology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.ORCID 0000-0002-9092-2265
Edward V MaytinDepartment of Dermatology and Department of Biomedical Engineering, Cleveland Clinic, Cleveland, Ohio.
Imran RizviWellman Center for Photomedicine, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.ORCID 0000-0001-9673-4700
Tayyaba HasanWellman Center for Photomedicine, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts. thasan@mgh.harvard.edu.
Massachusetts General Hospital · USCleveland Clinic · USNYU Langone Health · USThe University of Texas Health Science Center at San Antonio · US

Funding

Small Molecule Enhancers of Photodynamic Therapy for Skin CancerP01CA084203 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI Bryan Quilty Spring · 2001 to 2026
$27.9M
Low-cost Enabling Technology for Image-guided Photodynamic Therapy (PDT) of OralUH3CA189901 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI CELLI, JONATHAN P, HASAN, TAYYABA · 2016 to 2019
$2.7M
VisualSonics Photoacoustic and Ultrasound Imaging SystemS10OD012326 · OD · MASSACHUSETTS GENERAL HOSPITAL · PI HASAN, TAYYABA · 2012 to 2012
$912k
Targeting Determinants of OvCa Metastases in Engineered 3D Microfluidic PlatformsR00CA175292 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI RIZVI, IMRAN · 2016 to 2019
$746k
Multifunctional, GBM-Activatable Nanocarriers For Image-Guided PhotochemotherapyR00CA194269 · NCI · UNIV OF MARYLAND, COLLEGE PARK · PI HUANG, HUANG CHIAO · 2018 to 2020
$701k
Multifunctional, GBM-activatable nanocarriers for image-guided photochemotherapyK99CA194269 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI HUANG, HUANG CHIAO · 2016 to 2017
$358k
Targeting Determinants of OvCa Metastases in Engineered 3D Microfluidic PlatformsK99CA175292 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI RIZVI, IMRAN · 2014 to 2015
$350k
Howard Hughes Medical InstituteNCI NIH HHS K99 CA175292NCI NIH HHS K99 CA194269NCI NIH HHS P01 CA084203NCI NIH HHS R00 CA175292NCI NIH HHS R00 CA194269NCI NIH HHS UH3 CA189901NIH HHS S10 OD012326
6 · The paper itself

Abstract

Patients with cancer often confront the decision of whether to continue high-dose chemotherapy at the expense of cumulative toxicities. Reducing the dose of chemotherapy regimens while preserving efficacy is sorely needed to preserve the performance status of these vulnerable patients, yet has not been prioritized. Here, we introduce a dual pronged approach to modulate the microenvironment of desmoplastic pancreatic tumors and enable significant dose deescalation of the FDA-approved chemotherapeutic nanoliposomal irinotecan (nal-IRI) without compromising tumor control. We demonstrate that light-based photodynamic priming (PDP) coupled with vitamin D3 receptor (VDR) activation within fibroblasts increases intratumoral nal-IRI accumulation and suppresses protumorigenic CXCL12/CXCR7 crosstalk. Combined photodynamic and biochemical modulation of the tumor microenvironment enables a 75% dose reduction of nal-IRI while maintaining treatment efficacy, resulting in improved tolerability. Modifying the disease landscape to increase the susceptibility of cancer, via preferentially modulating fibroblasts, represents a promising and relatively underexplored strategy to enable dose deescalation. The approach presented here, using a combination of three clinically available therapies with nonoverlapping toxicities, can be rapidly translated with minimal modification to treatment workflow, and challenges the notion that significant improvements in chemotherapy efficacy can only be achieved at the expense of increased toxicity.

Indexed as

Gene Expression Regulation, NeoplasticPhotochemotherapyAnimalsAntineoplastic AgentsApoptosisBiomarkers, TumorCalcitriolCarcinoma, Pancreatic DuctalCell ProliferationChemokine CXCL12Dermatologic AgentsHumansMaleMiceMice, NudePancreatic NeoplasmsACKR3 protein, humanAntineoplastic AgentsBiomarkers, TumorcalcipotrieneCalcitriolChemokine CXCL12CXCL12 protein, humanCXCR4 protein, humanDermatologic AgentsReceptors, CalcitriolReceptors, CXCRReceptors, CXCR4VDR protein, human

Identifiers

PMID32220968
PMCPMC7272264
OpenAlexW3013440946

What OpenQuestion holds

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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.