Evidence map›Paper›PMID 38449313›Full record

ReviewMolecular therapy : the journal of the American Society of Gene Therapy2024

Engineering small-molecule and protein drugs for targeting bone tumors.

Yixian Wang, Chenhang Wang, Meng Xia, Zeru Tian, Joseph Zhou, Julian Meyer Berger, Xiang H-F Zhang, Han Xiao

Open access · greenAbstract readReview
In one paragraph

Review in Molecular therapy : the journal of the American Society of Gene Therapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

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  13. Role of miRNA‑122 in cancer (Review).International journal of oncology · 2024
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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

8 authors at 3 institutions in 1 country.

Yixian WangDepartment of Chemistry, Rice University, 6100 Main Street, Houston, TX 77005, USA.
Chenhang WangDepartment of Chemistry, Rice University, 6100 Main Street, Houston, TX 77005, USA.
Meng XiaDepartment of Chemistry, Rice University, 6100 Main Street, Houston, TX 77005, USA.
Zeru TianDepartment of Chemistry, Rice University, 6100 Main Street, Houston, TX 77005, USA.
Joseph ZhouDepartment of Chemistry, Rice University, 6100 Main Street, Houston, TX 77005, USA.
Julian Meyer BergerOsteologic Therapeutics, Inc., 228 Park Ave S PMB 35546, New York, NY 10003, USA.
Xiang H-F ZhangDepartment of Molecular and Cellular Biology, Baylor College of Medicine, 1 Baylor Plaza, Houston, TX 77030, USA.
Han XiaoDepartment of Chemistry, Rice University, 6100 Main Street, Houston, TX 77005, USA; SynthX Center, Rice University, 6100 Main Street, Houston, TX 77005, USA; Department of Biosciences, Rice University, 6100 Main Street, Houston, TX 77005, USA; Department of Bioengineering, Rice University, 6100 Main Street, Houston, TX 77005, USA. Electronic address: han.xiao@rice.edu.
Rice University · USBaylor College of Medicine · USIo Therapeutics (United States) · US

Funding

Engineering Proteins with Noncanonical Amino AcidsR35GM133706 · NIGMS · RICE UNIVERSITY · PI Han Xiao · 2019 to 2026
$2.9M
Modulation of Epigenetic Target in the Bone to Treat Breast Cancer MetastasisR01CA277838 · NCI · RICE UNIVERSITY · PI Han Xiao, Xiang Zhang · 2023 to 2026
$2.6M
Development of Bone-Targeting Antibodies for Ewing Sarcoma Using Genetic Code ExpansionR21CA255894 · NCI · RICE UNIVERSITY · PI XIAO, HAN, YUSTEIN, JASON · 2021 to 2023
$568k
NCI NIH HHS R01 CA277838NCI NIH HHS R21 CA255894NIGMS NIH HHS R35 GM133706
6 · The paper itself

Abstract

Bone cancer is common and severe. Both primary (e.g., osteosarcoma, Ewing sarcoma) and secondary (e.g., metastatic) bone cancers lead to significant health problems and death. Currently, treatments such as chemotherapy, hormone therapy, and radiation therapy are used to treat bone cancer, but they often only shrink or slow tumor growth and do not eliminate cancer completely. The bone microenvironment contributes unique signals that influence cancer growth, immunogenicity, and metastasis. Traditional cancer therapies have limited effectiveness due to off-target effects and poor distribution on bones. As a result, therapies with improved specificity and efficacy for treating bone tumors are highly needed. One of the most promising strategies involves the targeted delivery of pharmaceutical agents to the site of bone cancer by introduction of bone-targeting moieties, such as bisphosphonates or oligopeptides. These moieties have high affinities to the bone hydroxyapatite matrix, a structure found exclusively in skeletal tissue, and can enhance the targeting ability and efficacy of anticancer drugs when combating bone tumors. This review focuses on the engineering of small molecules and proteins with bone-targeting moieties for the treatment of bone tumors.

Indexed as

Antineoplastic AgentsBone NeoplasmsAnimalsDiphosphonatesDrug Delivery SystemsHumansMolecular Targeted TherapyOsteosarcomaSarcoma, EwingTumor MicroenvironmentAntineoplastic AgentsDiphosphonatesbisphosphonatebonebone metastasisbone-targetingbone tumor

Identifiers

PMID38449313
PMCPMC11081876
OpenAlexW4392516483

What OpenQuestion holds

Textmetadata
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.