funder-graph

FundersMN

Grants paid by A Breath of Hope Lung Foundation

EIN 30-0475578 · Bloomington, MN · Form 990, Schedule I · NTEE G123

A Breath of Hope Lung Foundation of Bloomington, MN (EIN 30-0475578) reported 21 grants paid totaling $1,200,000 to 10 recipients in tax years 2018–2025, on Form 990, Schedule I. Derived from IRS e-file data, dataset version 2026.09.0, built 2026-09-03.

Grants paid

$1,200,000

21 grants

Recipients

10

distinct organizations

Tax years

2018–2025

8 filings in the corpus

By tax year

Grants by tax year, as the same figures
Tax yearGrants paidAmount paidApproved for future
20183$150,000
20192$150,000
20202$75,000
20212$150,000
20223$150,000
20231$75,000
20244$187,500
20254$262,500

Top recipients

The 10 recipients receiving the most from A Breath of Hope Lung Foundation, by grants paid, out of 10 distinct recipients.

Recipients ranked by total grants paid
RecipientMatchLocationGrantsTotal paidLatest year
Mayo Clinic 41-6011702ARochester, MN2$150,0002025
Massachusetts Institute of Technology 04-2103594ACambridge, MA3$150,0002020
Massachusetts General Hospital 04-1564655ABoston, MA3$150,0002024
University of Pittsburgh 25-0965591APittsburgh, PA2$150,0002019
Whitehead Institute of Biomedical Research 60-1043412ACambridge, MA2$150,0002022
University of Texas Southwestern 75-6002868ADallas, TX3$150,0002022
Albert Einstein College of Medicine 83-0621846ABronx, NY2$112,5002025
Emory University 58-0566256AAtlanta, GA2$112,5002025
University of Texas at Austin 74-6000203AAustin, TX1$37,5002025
Nyu School of Medicine 13-3971298ABoston, MA1$37,5002018

Match tier: A Reported EIN · B Exact name and place · C Strong name match · D Probable name match · U Unresolved. Tiers C and D are inferred, not reported; see how matching works.

Every grant

All 21 grant rows this organization reported, most recent first.

Grants reported by A Breath of Hope Lung Foundation
Tax yearRecipientMatchAmountTypePurposeSource filing
2025Mayo Clinic Rochester, MNA$75,000paid2023 Peg's Fight for Life Award202621079349300837
2025Emory University Atlanta, GAA$75,000paid2024 Julie Swedberg YOLO Award202621079349300837
2025Albert Einstein College of Medicine Bronx, NYA$75,000paid2024 Peg's Fight for Life Award202621079349300837
2025University of Texas at Austin Austin, TXA$37,500paid2025 Peg's Fight for Life Award202621079349300837
2024Mayo Clinic Rochester, MNA$75,000paid2023 Peg's Fight for Life Award202501059349302800
2024Albert Einstein College of Medicine Bronx, NYA$37,500paid2024 Peg's Fight for Life Award202501059349302800
2024Emory University Atlanta, GAA$37,500paidJulie Swedberg YOLO Award202501059349302800
2024Massachusetts General Hospital Boston, MAA$37,500paid2022 Peg's Fight for Life Award202501059349302800
2023Massachusetts General Hospital Boston, MAA$75,000paidPegs Fight for Life Award202431309349302208
2022Whitehead Inst for Biomedical Cambridge, MAA$75,000paidPeg Fisher 2021 Research Award202341329349305689
2022Massachusetts General Boston, MAA$37,500paidPegs Fight for Life Award202341329349305689
2022Univ of Texas Sw Medical Dallas, TXA$37,500paidKatherine Bensen Hope Award202341329349305689
2021Whitehead Institute of Biomedical Research Cambridge, MAA$75,000paidThis research project focuses on improving lung cancer outcomes with two aims: 1) To determine the mechanism by which macrophage activation enhances the response to EGFR TKIs; and 2: To investigate the anti-tumor efficacy of EGFR TKIs in combination with macrophage-directed therapies in xenograft models.202221229349301267
2021University of Texas Southwestern Dallas, TXA$75,000paidThe research project is seeking to understand the role of Telmerase that is expressed by most human cancers, particularly small cell lung cancer. We will target an essential survival mechanism of tumor cells to activate protective antitumor immunity and immune memory. We hypothesize that sytosolic DNA resulting from targeting telmerase with 6TdG treatment induces the cGAS/STING pathway, leading to enhanced antigen presentation and cyokine expression from tumors and dendritic cells (DC), causing the expansion and activation of tumor-specific T cells. If successful, our studies will guide the design of clinical trials. Given that NIH considers SCLC a recalcitrant disease, we believe SCLCs can easily be prioritized to be one of the first cancers to test 6TdG as these tumors do not have effective treatments currently. If we can generate strong preclinical evidence with this proposal, 6TdG can rapidly move in this subset in the clinic.202221229349301267
2020University of Texas Southwestern Dallas, TXA$37,500paidThe research project is seeking to understand the role of Telomerase that is expressed by most human cancers, particularly small cell lung cancer. We will target an essential survival mechanism of tumor cells to activate protective antitumor immunity and immune memory. We hypothesize that cytosolic DNA resulting from targeting telomerase with 6TdG treatment induces the cGAS/STING pathway, leading to enhanced antigen presentation and cytokine expression from tumors and dendritic cells (DC), causing the expansion and activation of tumor-specific T cells. If successful, our studies will guide the design of clinical trials. Given that NIH considers SCLC a recalcitrant disease, we believe SCLCs can easily be prioritized to be one of the first cancers to test 6TdG as these tumors do not have effective treatments currently. If we can generate strong preclinical evidence with this proposal, 6TdG can rapidly move in this subset in the clinic.202131119349301503
2020Massachusetts Institute of Technology Cambridge, MAA$37,500paidThe research project is seeking to tackle a long-standing question on whether the heterogeneity of a tumor is impacting its immune response. Although often perceived as one disease, any cancer lesion is comprised of millions of tumor cells. While some tumor cells seem similar to others, they may be very different in their appearance to the immune system. This phenomenon of high intra-tumor heterogeneity is particularly common in lung cancer. Despite us knowing about the heterogeneity, we currently have no mechanistic understanding of its impact on anti-tumor immunity. Understanding this interplay will help find rational and potent combination treatments with cancer immunotherapy, a relatively new treatment modality activating the patient's own immune system to fight cancer.202131119349301503
2019Massachusetts Institute of Technology Cambridge, MAA$75,000paidLung cancer research grant: The research project funded by A Breath of Hope Lung Foundation is seeking to tackle a long-standing question on whether the heterogeneity of a tumor is impacting its immune response. Although often perceived as one disease, any cancer lesion is comprised of millions of tumor cells. While some tumor cells seem similar to others, they may be very different in their appearance to the immune system. This phenomenon of high intra-tumor heterogeneity is particularly common in lung cancer. Despite us knowing about the heterogeneity, we currently have no mechanistic understanding about its impact on anti-tumor immunity. Understanding this interplay will help find rational and potent combination treatments with cancer immunotherapy, a relatively new treatment modality activating the patients' own immune system to fight cancer.202001419349301465
2019University of Pittsburgh Pittsburgh, PAA$75,000paidLung cancer research grant: Lung cancer is the leading cause of cancer death in women, killing more women each year than breast, uterine and ovarian cancers combined. Sex differences in non-small cell lung cancer (NSCLC) and survival suggest that estrogen plays a critical factor in the formation of tumors in women's lungs. Preclinical and epidemiological studies have demonstrated that the estrogen pathway is a driver of NSCLC progression in women. Results of this project will provide a mechanistic understanding of the role of estrogen on immune suppression and whether hormonal blockade can improve the response rate or durability of response in women with this type of cancer that are treated with targeted immunotherapy.202001419349301465
2018University of Pittsburgh Pittsburgh, PAA$75,000paidLung cancer research201921359349314512
2018Nyu School of Medicine Boston, MAA$37,500paidLung cancer research201921359349314512
2018Massachusetts Institute of Technology Cambridge, MAA$37,500paidLung cancer research201921359349314512

Match tier: A Reported EIN · B Exact name and place · C Strong name match · D Probable name match · U Unresolved. Tiers C and D are inferred, not reported; see how matching works.

Recipient matching for this dataset version has not yet completed its independent precision check. Tier A rows carry the EIN the filer reported; tiers B–D are the matcher's inference and should be read as leads until the check is published on the methodology page.

Source filings

Every figure above is traceable to one of these IRS e-file returns by its OBJECT_ID.

Returns this page is derived from
FormTax yearPeriod endFiledSchemaIRS OBJECT_ID
99020252025-12-31not stated2025v4.1202621079349300837
99020242024-12-31not stated2024v5.0202501059349302800
99020232023-12-31not stated2023v5.0202431309349302208
99020222022-12-31not stated2022v5.0202341329349305689
99020212021-12-31not stated2021v4.0202221229349301267
99020202020-12-31not stated2020v4.0202131119349301503
99020192019-12-31not stated2019v5.0202001419349301465
99020182018-12-31not stated2018v3.0201921359349314512

Derived from IRS Form 990 e-file XML; recipient identities from the IRS Exempt Organizations Business Master File. Dataset version 2026.09.0, built 2026-09-03. The same rows as Parquet: manifest; as JSON: /api/funders/300475578.json.

The same organization elsewhere in the program: exempt status and filing health · federal awards · grant guidance · open opportunities.

This is informational only, derived from public data on the dates shown. It is not an eligibility determination, and not legal, tax, or accounting advice. Verify against the official source before relying on it.