Article in Cancer discovery, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
0numbers the graph read from it
0cells of the map it votes in
7citing 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.
Julie E LangDivision of Breast Cancer, Department of Cancer Biology, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio.ORCID 0000-0002-7534-6124
Tumor BiologyP30CA125123 · NCI · BAYLOR COLLEGE OF MEDICINE · PI Michael M Ittmann · 2007 to 2026
$73.9M
THE TISCH CANCER INSTITUTE - CANCER CENTER SUPPORT GRANTP30CA196521 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Ramon E Parsons · 2015 to 2026
$35.4M
NIH FIRST Cohort Cluster Hiring Initiative at Icahn School of Medicine at Mount SinaiU54CA267776 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Nihal Mohamed · 2021 to 2026
$17.4M
Osteoclast-Independent Mechanisms of Early-Stage Bone Colonization of Breast CancerR01CA183878 · NCI · BAYLOR COLLEGE OF MEDICINE · PI ZHANG, XIANG · 2014 to 2024
$3.5M
Spatiotemporal modeling of cancer-niche interactions in breast cancer bone metastasisU01CA253553 · NCI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI WONG, STEPHEN TC, ZHANG, XIANG · 2020 to 2024
$3.0M
Unveiling the mechanisms underlying secondary metastasis and possible therapeutic windowsR01CA251950 · NCI · BAYLOR COLLEGE OF MEDICINE · PI ZHANG, XIANG · 2020 to 2024
$2.6M
Chronic Mitochondrial Division and Melanoma: Mechanism, Prognosis, and TherapyR01CA267696 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Jerry Edward Chipuk · 2022 to 2026
$2.4M
The Oncogene Activated Mitochondrial Unfolded Protein Response Regulates Senescence BiologyR01CA271346 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Jerry Edward Chipuk · 2023 to 2026
$2.4M
COVID and Translational Science supercomputer (CATS)S10OD030463 · OD · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI KOVATCH, PATRICIA · 2021 to 2021
$2.0M
Big Omics Data Engine 2 SupercomputerS10OD026880 · OD · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI KOVATCH, PATRICIA · 2019 to 2019
$2.0M
Function and Regulation of the BCL-2 FamilyR01CA237264 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI CHIPUK, JERRY EDWARD · 2020 to 2024
$1.9M
Tracing and targeting the epigenetic heterogeneity in breast cancer metastasisR00CA263033 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI BADO, IGOR LANDRY · 2022 to 2024
$688k
Breast Cancer Alliance (BCA)Breast Cancer Research Foundation (BCRF) 23-20-26-BADOCancer Prevention and Research Institute of Texas (CPRIT) CPRIT-RP180672Common Fund (NIH Common Fund) U54CA267776National Cancer Institute (NCI) K99CA263033-01A1National Cancer Institute (NCI) R01CA183878National Institutes of Health (NIH) P30CA196521NCI NIH HHS K99 CA263033NCI NIH HHS P30 CA125123NCI NIH HHS P30 CA196521NCI NIH HHS R00 CA263033NCI NIH HHS R01 CA183878NCI NIH HHS R01 CA237264NCI NIH HHS R01 CA251950NCI NIH HHS R01 CA267696NCI NIH HHS R01 CA271346NCI NIH HHS U01 CA253553NCI NIH HHS U54 CA267776NCRR NIH HHS S10 RR024574NIH HHS S10 OD018033NIH HHS S10 OD023469NIH HHS S10 OD025240NIH HHS S10 OD026880NIH HHS S10 OD030463U.S. Department of Defense (DOD) BC201371P1U.S. Department of Defense (DOD) W81XWH-21-1-0790
6 · The paper itself
Abstract
significanceGiven the urgent need for alternative strategies to block metastasis progression, we demonstrate that blocking HER2-mediated secondary metastasis improves clinical outcome and establish HER2 as a biomarker for bone metastasis in patients with initial HR+/HER2- breast cancer, which represents ∼70% of all cases.
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.
Bone-Induced HER2 Promotes Secondary Metastasis in HR+/HER2- Breast Cancer. · full record | OpenQuestion