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Links from GEO DataSets

Items: 4

1.
Full record GDS4330

Long-term octreotide treatment of neuroendocrine tumor cell line CNDT2.5

Analysis of ileum neuroendocrine tumor (NET) cell line CNDT2.5 treated with octreotide for up to 16 months. Somatostain analog octreotide is used to treat NET patients. Results provided insight into molecular basis of successful octreotide therapy or the development of drug resistance in NETs.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 2 agent, 5 cell line, 3 time sets
Platform:
GPL6244
Series:
GSE24358
8 Samples
Download data: CEL, CHP
2.

Gene expression profiling of neuroendocrine primary tumors: effect of Octreotide treatment

(Submitter supplied) The management of neuroendocrine tumors (NETs) is very variable, depending on many specific aspects, such as the type of tumor, spread and patient general health. Several advances have been made with the newly developed somatostatin analogues to cure this type of malignancies. Somatostain analogues such as octreotide have been used in clinic to treat patients with neuroendocrine tumors (NETs). However, the molecular mechanism leading either to successful therapy or acquired resistance to the analogues is still to large extent unclear. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS4330
Platform:
GPL6244
8 Samples
Download data: CEL, CHP
Series
Accession:
GSE24358
ID:
200024358
3.

Optimization of 177Lu-octreotate treatment of neuroendocrine tumours

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens; Mus musculus
Type:
Expression profiling by array
Platforms:
GPL10558 GPL6885
87 Samples
Download data
Series
Accession:
GSE80024
ID:
200080024
4.

Exposure to the olfactory receptor 51E1 agonist nonanoic acid alters small intestinal neuroendocrine tumor phenotype

(Submitter supplied) This study explores the hypothesis that stimulating the chemo-sensing olfactory receptor 51E1 (OR51E1) decreases SI-NET proliferation suggesting a mechanism that explains a difference in proliferative rate based on tumor location
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
2 Samples
Download data: XLSX
Series
Accession:
GSE216067
ID:
200216067
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