Cited by 6Drug Transport and Resistance MechanismsCancer Treatment and PharmacologyColorectal Cancer Treatments and Studies

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Data on the in vitro and in vivo anti-tumor effects of itraconazole, paclitaxel, and the two in combination in HT-29 and YM-1 cancer cell line and HT-29 colon cancer xenograft models

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Ghadi, Mahdi, Hosseinimehr, Seyed Jalal, Talebpour Amiri, Fereshteh, Mardanshahi, Alireza, Noaparast, Zohreh·2021·Data in Brief

Abstract

Colon cancer is one of the fatal cancers in the world that metastatic potential and resistance to chemotherapy drugs are outstanding causes of cancer-induced mortality [1], [2], [3], [4]. We have investigated in vitro and in vivo anti-cancer effect of itraconazole and paclitaxel alone and their anti-cancer synergistic effect through MTT assay in YM-1 and HT-29 cell lines and in HT-29 tumor-bearing nude mice. Histopathological experiment was done for further assessment. Also, we evaluated the inhibitory effect of itraconazole on P-gp using specific in vivo biodistribution through 99mTc-MIBI uptake. 99mTc-MIBI, a myocardial perfusion imaging agent, is a useful radiotracer in diagnosis of some tumors and the liver and tumor accumulation of 99mTc-MIBI is changed by P-gp regulators [5], [6], [7], [8]. The data presented in this article are related to the research paper entitled “Itraconazole synergistically increases therapeutic effect of paclitaxel and 99mTc-MIBI accumulation, as a probe of P-gp activity, in HT-29 tumor-bearing nude mice”. We hope our preliminary data to be helpful to design the chemotherapy regimen schedule with Itraconazole and Paclitaxel.

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Crossref · 10.1016/j.dib.2021.106862

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Fig. 1 Histopathologic findings of liver tissue A: Itraconazole (20 mg/Kg) group B: Itraconazole (20 mg/Kg) + Paclitaxel (20 mg/Kg) group. Hepatic cells showed increased inflammatory cells in itraconazole + paclitaxel groups but were only lower than those in itraconazole 20 mg / kg. H&E staining, Magnification: 40×, Scale bar: 100µm.
Fig. 1 Histopathologic findings of liver tissue A: Itraconazole (20 mg/Kg) group B: Itraconazole (20 mg/Kg) + Paclitaxel (20 mg/Kg) group. Hepatic cells showed increased inflammatory cells in itraconazole + paclitaxel groups but were only lower than those in itraconazole 20 mg / kg. H&E staining, Magnification: 40×, Scale bar: 100µm.CC BY-NC-ND · PubMed Central

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Metadata

Authors
Ghadi, M., Hosseinimehr, S. J., Talebpour Amiri, F., Mardanshahi, A., & Noaparast, Z.
Affiliations
Mazandaran University of Medical Sciences (IR)
Corresponding author
Noaparast, Zohreh
Venue
Data in Brief
Publisher
Elsevier BV
Published
2021-04
Volume
35
Pages
106862
ISSN
2352-3409 (ISSN-L)
OpenAlex
W3132061907
Cited by
6
References
11
Citations by year
2026: 2 · 2025: 2 · 2023: 1 · 2022: 1
Type
data paper
Language
en
Open access
Locations
  • Data in Brief (publishedVersion, cc-by-nc-nd)
  • PubMed Central (publishedVersion, cc-by-nc-nd)
  • PubMed (publishedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
Funders
Mazandaran University of Medical Sciences
Topics
  • Health Sciences › Medicine › Oncology › Drug Transport and Resistance Mechanisms
  • Health Sciences › Medicine › Oncology › Cancer Treatment and Pharmacology
  • Health Sciences › Medicine › Oncology › Colorectal Cancer Treatments and Studies
Keywords
itraconazole, paclitaxel, colon cancer, drug synergy, P-glycoprotein, tumor xenografts, HT-29 cells, chemoresistance, anticancer activity

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