Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: UMLS:C0018133 (
graft-versus-host disease
)
18,032
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Non-gestational choriocarcinoma (NGC) is a rare subtype of choriocarcinoma differing in origin and phenotypic characteristics compared to gestational choriocarcinoma (GC). This study aimed to analyze the molecular biology of GC and NGC and evaluate genetic anomalies of choriocarcinoma subtypes. DNA was extracted and paired from tumor-normal tissue of one NGC and one GC (control) patient for whole-exome sequencing. To further understand the role of
DNAJB9
, a
p53
regulator mutated in the NGC tumor, on
p53
upregulation in choriocarcinoma, CRISPR/Cas9 was used to induce
DNAJB9
site-specific mutations in choriocarcinoma cells JEG-3. We hypothesized that
DNAJB9
dysfunction would result in
p53
overexpression. Sequencing revealed the GC tumor contained > 7 times more somatic mutations than the NGC tumor. Missense (98.86% vs. 94.97%), stop-gain (0.57% vs. 0.93%), and frameshift mutations (0.57% vs. 4.10%) were observed in the GC and NGC samples, respectively (
x
2
= 24.63,
P
< 0.00001). The transition substitution rate was 67.54% and 55.71% in the GC and NGC samples, while the transversion substitution rate was 32.46% and 44.29% in the GC and NGC samples, respectively (
x
2
= 11.56,
P
< 0.000673). Pathway enrichment analysis revealed ECM-receptor interaction and
graft-versus-host disease
were most enriched in the GC and NGC tumors, respectively.
In vitro
investigations showed that
DNAJB9
mRNA and protein levels were downregulated in Cas9-
DNAJB9
-sgRNA transfected cells compared to the control (
P
< 0.001), while
p53
protein levels were upregulated. Our findings display the genetic distinctness of choriocarcinoma subtypes, especially NGC, and further highlight the relationship between
p53
and
DNAJB9
in choriocarcinoma cells, laying the foundation for further investigations.
...
PMID:A pilot study comparing the genetic molecular biology of gestational and non-gestational choriocarcinoma. 3181 8