Evidence map›Paper›PMID 37047307›Full record

ArticleInternational journal of molecular sciences2023

Anticancer Activity of Novel Difluorinated Curcumin Analog and Its Inclusion Complex with 2-Hydroxypropyl-β-Cyclodextrin against Pancreatic Cancer.

Sangita Bhattacharyya, Hindole Ghosh, Obdulia Covarrubias-Zambrano, Krishan Jain, K Venkateswara Swamy, Anup Kasi, Ameer Hamza, Shrikant Anant, Michael VanSaun, Scott J Weir and 3 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. 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
1.6field-weighted citation impact, top 19% 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, 16 citations in OpenAlex.

  1. Review
  2. Article
  3. NovelCancer drug resistance (Alhambra, Calif.) · 2026
    Article
  4. Review
  5. Mitigating Mucoadhesion of β-Cyclodextrins via PEGylation: Insights fromInternational journal of molecular sciences · 2025
    Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Review
  12. Review
  13. 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

13 authors at 4 institutions in 2 countries.

Sangita BhattacharyyaDepartment of Cancer Biology, University of Kansas Medical Center, Kansas City, KS 66103, USA.
Hindole GhoshDepartment of Cancer Biology, University of Kansas Medical Center, Kansas City, KS 66103, USA.
Obdulia Covarrubias-ZambranoDepartment of Cancer Biology, University of Kansas Medical Center, Kansas City, KS 66103, USA.
Krishan JainDepartment of Cancer Biology, University of Kansas Medical Center, Kansas City, KS 66103, USA.ORCID 0000-0002-1392-7038
K Venkateswara SwamyMIT School of Bioengineering, Sciences & Research, MIT Art, Design and Technology University, Pune 412201, India.
Anup KasiDivision of Medical Oncology, University of Kansas, Kansas City, KS 66160, USA.
Ameer HamzaPathology and Laboratory Medicine, University of Kansas, Kansas City, KS 66160, USA.ORCID 0000-0001-6158-4861
Shrikant AnantDepartment of Cancer Biology, University of Kansas Medical Center, Kansas City, KS 66103, USA.ORCID 0000-0003-4193-3053
Michael VanSaunDepartment of Cancer Biology, University of Kansas Medical Center, Kansas City, KS 66103, USA.
Scott J WeirDepartment of Cancer Biology, University of Kansas Medical Center, Kansas City, KS 66103, USA.ORCID 0000-0002-8020-434X
Stefan H BossmannDepartment of Cancer Biology, University of Kansas Medical Center, Kansas City, KS 66103, USA.
Subhash B PadhyeDepartment of Cancer Biology, University of Kansas Medical Center, Kansas City, KS 66103, USA.
Prasad DandawateDepartment of Cancer Biology, University of Kansas Medical Center, Kansas City, KS 66103, USA.ORCID 0000-0002-1141-3703
The University of Kansas Cancer Center · USMIT Art, Design and Technology University · INUniversity of Kansas · USUniversity of Kansas Medical Center · US

Funding

Transgenic & Gene-Targeting Shared ResourceP30CA168524 · NCI · UNIVERSITY OF KANSAS MEDICAL CENTER · PI ROY A. JENSEN · 2012 to 2026
$40.1M
XRAY CRYSTALLOGRAPHY CORE (JANUARY 1 - JUNE 30, 2005)P20RR016443 · NCRR · UNIVERSITY OF KANSAS MEDICAL CENTER · PI STEPHENS, EDWARD BRICE · 2001 to 2010
$21.3M
Mechanisms mediating resistance to ibrutinib in Non-Hodgkin's lymphomaR01CA201135 · NCI · SEATTLE CHILDREN'S HOSPITAL · PI JAMES, RICHARD GOFF · 2017 to 2021
$2.1M
American Gastroenterological Association 2021RSA-12522Council of Scientific and Industrial Research Senior Research FellowNCI NIH HHS P30 CA168524NCI NIH HHS R01 CA201135NCRR NIH HHS P20 RR016443The University of Kansas Cancer Center P30CA168524-01United States Department of Defense CA201135
6 · The paper itself

Abstract

Pancreatic ductal adenocarcinoma (PDAC) is the primary reason for cancer-related deaths in the US. Genetic mutations, drug resistance, the involvement of multiple signaling pathways, cancer stem cells (CSCs), and desmoplastic stroma, which hinders drug penetrance, contribute to poor chemotherapeutic efficacy. Hence, there is a need to identify novel drugs with improved delivery to improve treatment outcomes. Curcumin is one such compound that can inhibit multiple signaling pathways and CSCs. However, curcumin's clinical applicability for treating PDAC is limited because of its poor solubility in water and metabolic instability. Hence, we developed a difluorinated curcumin (CDF) analog that accumulates selectively in the pancreas and inhibits PDAC growth in vitro and in vivo. In the present work, we developed its 2-hydroxy-propyl-β-cyclodextrin (HCD) inclusion complex to increase its water solubility and hydrolytic stability. The CDFHCD inclusion complex was characterized by spectroscopic, thermal, and microscopic techniques. The inclusion complex exhibited increased aqueous solubility, hydrolytic stability, and antiproliferative activity compared to parent CDF. Moreover, CDF and CDFHCD inhibited colony and spheroid formation, and induced cell cycle and apoptosis in PDAC cell lines. Hence, CDFHCD self-assembly is an efficient approach to increase water solubility and anticancer therapeutic efficacy, which now warrants advancement towards a clinical proof of concept in PDAC patients.

Indexed as

Carcinoma, Pancreatic DuctalCurcuminPancreatic Neoplasms2-Hydroxypropyl-beta-cyclodextrinHumansSolubilityWater2-Hydroxypropyl-beta-cyclodextrinCurcuminWater2-hydroxypropyl-β-cyclodextrinCDFcurcumincyclodextrindifluorinated curcuminpancreatic cancerPDAC

Identifiers

PMID37047307
PMCPMC10093935
OpenAlexW4361219378

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.