1989
DOI: 10.1007/bf02628465
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Further cellular investigation of the human hepatoblastoma-derived cell line HepG2: Morphology and immunocytochemical studies of hepatic-secreted proteins

Abstract: The hepatoblastoma cell line HepG2 has been a matter of many investigations; most of them include biochemical studies of lipoprotein and other hepatic protein metabolism. However, the accurate cellular features of these cells have not been emphasized. We studied the cellular histologic, histochemical, and ultrastructural characteristics of this cell line. In addition, we investigated by immunoenzymatic methods the cellular biosynthesis of several proteins: apolipoproteins-AI, -B, -D, and -E, albumin, alpha-fet… Show more

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Cited by 116 publications
(83 citation statements)
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“…Indeed, our late passage cells showed a number of genetic abnormalities, including aneuploidy (data not shown) that are characteristic of senescent cultures. The possibility that CRET elicits antiproliferative effects in senescent ADSC could take partial support from previous studies by our group, which report that CRET treatment causes antiproliferative effects in hepatocarcinoma HepG2 and neuroblastoma NB69 [32,33,34,35,36], two human cancer cell lines known to carry a variety of genetic alterations [52,53]. …”
Section: Discussionsupporting
confidence: 48%
“…Indeed, our late passage cells showed a number of genetic abnormalities, including aneuploidy (data not shown) that are characteristic of senescent cultures. The possibility that CRET elicits antiproliferative effects in senescent ADSC could take partial support from previous studies by our group, which report that CRET treatment causes antiproliferative effects in hepatocarcinoma HepG2 and neuroblastoma NB69 [32,33,34,35,36], two human cancer cell lines known to carry a variety of genetic alterations [52,53]. …”
Section: Discussionsupporting
confidence: 48%
“…24 Hepatoblastoma cells. The Hep G2/C3A clone of human hepatoblastoma cells 25 was obtained from American Type Culture Collection (Rockville, MD) (ATCC catalog #CRL-10791). The cells were grown at 37ЊC in minimum essential medium (Eagle) supplemented with 10% fetal bovine serum, 0.29 mg/ml of L-glutamine, 100 U/ml of penicillin G, 100 g/ml of streptomycin sulfate, and 1.5 mg/ml of sodium bicarbonate.…”
Section: Methodsmentioning
confidence: 99%
“…Firstly, while HepG2 cells have been well characterized (37-40), they may not be representative of normal hepatic tissue (41)(42)(43)(44) or hepatic tissue in PCOS patients. It is also possible that alternative effects of the factors added to the media may have affected our results.…”
Section: Discussionmentioning
confidence: 99%