Evidence map›Paper›PMID 37576871›Full record

ReviewMaterials today. Bio2023

Tumor-targeted liposomes with platycodin D2 promote apoptosis in colorectal cancer.

Euni Cho, Seok-Jun Mun, Minha Jeon, Hyo Keun Kim, Hwira Baek, Yu Seong Ham, Woo Jin Gil, Jin Woong Kim, Chul-Su Yang

Open access · goldAbstract readReview
In one paragraph

Review in Materials today. Bio, 2023. 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
1.8field-weighted citation impact, top 16% 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, 18 citations in OpenAlex.

  1. TMEM16F deficiency alleviates sepsis-induced acute lung injury through regulating macrophage polarization.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    Article
  2. Article
  3. Review
  4. Cancer chemoprevention: signaling pathways and strategic approaches.Signal transduction and targeted therapy · 2025
    Review
  5. Review
  6. Frontiers in nutrition · 2025
    Review
  7. Article
  8. Article
  9. 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

9 authors at 2 institutions in 1 country.

Euni ChoDepartment of Bionano Engineering Technology, Hanyang University, Seoul, 04673, South Korea.
Seok-Jun MunDepartment of Bionano Engineering Technology, Hanyang University, Seoul, 04673, South Korea.
Minha JeonSchool of Chemical Engineering, Sungkyunkwan University, Suwon, 16419, South Korea.
Hyo Keun KimCenter for Bionano Intelligence Education and Research, Ansan, 15588, South Korea.
Hwira BaekSchool of Chemical Engineering, Sungkyunkwan University, Suwon, 16419, South Korea.
Yu Seong HamCenter for Bionano Intelligence Education and Research, Ansan, 15588, South Korea.
Woo Jin GilCenter for Bionano Intelligence Education and Research, Ansan, 15588, South Korea.
Jin Woong KimSchool of Chemical Engineering, Sungkyunkwan University, Suwon, 16419, South Korea.
Chul-Su YangCenter for Bionano Intelligence Education and Research, Ansan, 15588, South Korea.
Hanyang University · KRSungkyunkwan University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Conventional chemotherapy for colorectal cancer (CRC), though efficacious, is discouraging due to its limited targeting capability, lack of selectivity, and chemotherapy-associated side effects. With the advent of nanomedicines, a liposomal delivery system making use of a combination of anticancer phytochemicals is fast gaining popularity as one of the most promising nanoplatforms for CRC treatment. Rising evidence supports phytochemicals such as platycosides for their anticancer potency. To this end, a combination therapy including tumor-targeted liposomes along with phytochemicals might have a greater therapeutic potential against cancer. In this study, we developed acidity-triggered rational membrane (ATRAM) along with conjugated platycodin D2 (PCD2) and liposomes (PCD2-Lipo-ATRAM) as a tumor-targeting therapy. The PCD2-Lipo-ATRAM treatment demonstrated a successful tumor-targeting ability in the CRC xenografts, in which PCD2 not only exerted a potent antitumor effect by inducing apoptotic cell death and but also functioned as a liposome membrane stabilizer. Moreover, PCD2-Lipo-ATRAM suppressed antiapoptotic BCL-2 family proteins, resulting in enhanced cytotoxicity toward CRC cells by inducing intrinsic caspase-9/-3 mediated apoptosis. Thus, our data has shown that tumor-targeting PCD2-based liposomal systems represent a promising strategy for CRC therapy, since they directly target the tumors, unlike other therapies that can miss the target.

Indexed as

ApoptosisColorectal cancerLiposomesPlatycosidesXenograft

Identifiers

PMID37576871
PMCPMC10415802
OpenAlexW4385383304

What Socratic 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 Socratic graph.