Evidence map›Paper›PMID 35355817›Full record

ArticleACS central science2022

Bone-Specific Enhancement of Antibody Therapy for Breast Cancer Metastasis to Bone.

Zeru Tian, Chenfei Yu, Weijie Zhang, Kuan-Lin Wu, Chenhang Wang, Ruchi Gupta, Zhan Xu, Ling Wu, Yuda Chen, Xiang H-F Zhang and 1 more

Open access · diamondAbstract read
In one paragraph

Article in ACS central science, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.6field-weighted citation impact, top 15% 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

9 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Metabolic reprogramming in bone metastasis of human cancers.Frontiers in cell and developmental biology · 2025
    Review
  7. Engineering small-molecule and protein drugs for targeting bone tumors.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Review
  8. Review
  9. Review
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

11 authors at 2 institutions in 1 country.

Zeru TianDepartment of Chemistry, Rice University, 6100 Main Street, Houston, Texas 77005, United States.
Chenfei YuDepartment of Chemistry, Rice University, 6100 Main Street, Houston, Texas 77005, United States.
Weijie ZhangLester and Sue Smith Breast Center, Baylor College of Medicine, 1 Baylor Plaza, Houston, Texas 77030, United States.
Kuan-Lin WuDepartment of Chemistry, Rice University, 6100 Main Street, Houston, Texas 77005, United States.
Chenhang WangDepartment of Chemistry, Rice University, 6100 Main Street, Houston, Texas 77005, United States.
Ruchi GuptaDepartment of Chemistry, Rice University, 6100 Main Street, Houston, Texas 77005, United States.
Zhan XuLester and Sue Smith Breast Center, Baylor College of Medicine, 1 Baylor Plaza, Houston, Texas 77030, United States.
Ling WuLester and Sue Smith Breast Center, Baylor College of Medicine, 1 Baylor Plaza, Houston, Texas 77030, United States.
Yuda ChenDepartment of Chemistry, Rice University, 6100 Main Street, Houston, Texas 77005, United States.
Xiang H-F ZhangLester and Sue Smith Breast Center, Baylor College of Medicine, 1 Baylor Plaza, Houston, Texas 77030, United States.
Han XiaoDepartment of Chemistry, Rice University, 6100 Main Street, Houston, Texas 77005, United States.ORCID https://orcid.org/0000-0002-4311-971X
Rice University · USBaylor College of Medicine · US

Funding

Osteogenic Niche Biology in Progression and Endocrine Resistance of Bone MetastasesR01CA221946 · NCI · BAYLOR COLLEGE OF MEDICINE · PI ROWLEY, DAVID R · 2018 to 2022
$2.4M
NCI NIH HHS R01 CA221946
6 · The paper itself

Abstract

Despite the rapid evolution of therapeutic antibodies, their clinical efficacy in the treatment of bone tumors is hampered due to the inadequate pharmacokinetics and poor bone tissue accessibility of these large macromolecules. Here, we show that engineering therapeutic antibodies with bone-homing peptide sequences dramatically enhances their concentrations in the bone metastatic niche, resulting in significantly reduced survival and progression of breast cancer bone metastases. To enhance the bone tumor-targeting ability of engineered antibodies, we introduced varying numbers of bone-homing peptides into permissive sites of the anti-HER2 antibody, trastuzumab. Compared to the unmodified antibody, the engineered antibodies have similar pharmacokinetics and

Identifiers

PMID35355817
PMCPMC8961797
OpenAlexW4220683979

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.