DLD-1

Cat.No.: CSC-C9371L

Species: Homo sapiens (Human)

Source: Intestine; Colon

Morphology: Epithelial

Culture Properties: monolayer

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Cat.No.
CSC-C9371L
Description
DLD-1 is one of two colorectal adenocarcinoma cell lines which were isolated by D.L. Dexter and associates during a period from 1977-1979. The cells have been used in the study of polar solvents on cell characteristics. The four cell lines: DLD-1, HCT-15, HCT-8 and HRT-18 have been shown to have a common genetic origin. DLD-1 can express carcinoembryonic antigen (CEA) 0.5 ng/106 cells/10 days and colon antigen 3. These cells are weakly positive for keratins and vimentin. The cells are positive for keratin by immunoperoxidase staining.
Species
Homo sapiens (Human)
Source
Intestine; Colon
Culture Properties
monolayer
Morphology
Epithelial
STR DNA Profile
Amelogenin: X,Y
CSF1PO: 11,12
D13S317: 8,11
D16S539: 12,13
D5S818: 13
D7S820: 10,12
THO1: 7,9.3
TPOX: 8,11
vWA: 18,19
Karyotype
This is a pseudodiploid human cell line with the modal chromosome number of 46, occurring in 86% of cells. The rate of polyploidy was high at 17.1%. The karyotype of the line was 46,XY,-2,+dir dup(2)(p13-p23). The Y chromosome was slightly longer than N22 and had a large segment of heterochromatic, fluorescent distal q arms.
Application
This cell line can be used as a suitable transfection host.
Disease
Colon Adenocarcinoma
Quality Control
Tests for mycoplasma, bacteria and fungi were negative
Storage and Shipping
Frozen with 52.5% RPMI-1640, 40% FBS, 7.5% DMSO at about 4-5 x 10^6 cells/ampoule; ship in dry ice; store in liquid nitrogen
Synonyms
DLD 1; DLD1; CoCL3
Citation Guidance
If you use this products in your scientific publication, it should be cited in the publication as: Creative Bioarray cat no. If your paper has been published, please click here to submit the PubMed ID of your paper to get a coupon.

DLD-1 is a human colorectal adenocarcinoma cell line established from a male patient with Dukes' C stage colon cancer. It was originally developed from epithelial tumor tissue from the colon. It demonstrates an adherent growth pattern and exhibits the polygonal, epithelial-like morphology typical of colon adenocarcinoma. DLD-1 is a genetically stable, well-characterized, and easy-to-culture cell line, frequently used as a general representative model for the in vitro study of colorectal cancer.

DLD-1 is notable for its well-characterized molecular profile, which includes KRAS G13D mutation, APC and PIK3CA mutations, and alterations in several major tumor-associated signaling pathways. This unique genomic signature makes DLD-1 an important model system to study oncogenic RAS and Wnt/β-catenin signaling, as well as drug resistance mechanisms and responses to targeted therapies.

DLD-1 functions as an in vitro model for various cancer cell processes including cell proliferation and metabolic reprogramming as well as apoptosis, autophagy, epithelial-mesenchymal transition and invasion mechanisms. The defined KRAS mutation status of this cell line also makes it a useful model to study resistance to anti-EGFR therapies, such as cetuximab and panitumumab.

The Effect of the Cardaria draba Subspecies Shalepensis Exerts on the Cell Viability of the Human Colon Cancer Cell Line (DLD-1)

Metabolic dysregulation and aberrant melanogenesis lead to hyperglycaemia and hyperpigmentation, respectively. Conventional treatments are often suboptimal. Ortaakarsu et al. investigated the inhibitory effects of Cardaria draba extract on α-glucosidase and tyrosinase-related protein 1, and its antiproliferative effects on DLD-1 colon cancer cells, to explore its potential as a therapeutic agent.

The cytotoxicity effect of the plant extract on Human Colon Cancer Cell Line (DLD-1) was evaluated by MTT method (Fig. 1). The viability values of DLD-1 cells were found to be 22.23% at 312 µg/mL and 38.94% at 625 µg/mL. The viability of cells at 1250 µg/mL was 87.61% and it decreased to 80.26% at 2500 µg/mL. The viability at 1250 and 2500 µg/mL increased, while at 312 and 625 µg/mL it decreased. Thus, the most suitable concentrations for DLD-1 were determined as 312 and 625 µg/mL. The IC50 value of DLD-1 cell line was found to be 767 µg/mL. ANOVA with Bonferroni corrections showed that the extract had significant effect. The change in trend at 2500 µg/mL was explained by the exceeding of threshold concentrations by the compounds of the extract, which causes a disturbance in the mechanisms that form the defense of the cell line.

The effect of the plant extract on the cell viability of the human Colon cancer cell line (DLD-1) during the 24-h experiment was observed.

Fig. 1. The effect of the plant extract on the cell viability of the human Colon cancer cell line (DLD-1) during the 24-h experiment was observed (Ortaakarsu A B, Boğa Ö B, et al., 2025).

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