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AN-152
Known as:
AEZS-108
National Institutes of Health
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Related topics
Related topics
2 relations
Broader (1)
LHRH, lysine(6)-doxorubicin
ZEN-008
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2013
Review
2013
Gonadotropin-releasing hormone receptors as molecular therapeutic targets in prostate cancer: Current options and emerging strategies.
P. Limonta
,
M. Manea
Cancer Treatment Reviews
2013
Corpus ID: 11288510
2009
2009
Luteinizing Hormone-Releasing Hormone Receptor-Targeted Chemotherapy Using AN-152
G. Emons
,
H. Sindermann
,
J. Engel
,
A. Schally
,
C. Gründker
Neuroendocrinology
2009
Corpus ID: 42396499
The luteinizing hormone-releasing hormone (LHRH; also known as gonadotropin-releasing hormone) receptor can be utilized for…
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Review
2004
Review
2004
Chemotherapy targeted to cancers through tumoral hormone receptors
A. Schally
,
A. Nagy
Trends in endocrinology and metabolism
2004
Corpus ID: 24687095
2003
2003
Preclinical evaluation of targeted cytotoxic luteinizing hormone-releasing hormone analogue AN-152 in androgen-sensitive and insensitive prostate cancers.
Markus Letsch
,
A. Schally
,
K. Szepesházi
,
G. Halmos
,
A. Nagy
Clinical Cancer Research
2003
Corpus ID: 16620016
PURPOSE AND EXPERIMENTAL DESIGN To improve conventional chemotherapy, we developed cytotoxic analogues of luteinizing hormone…
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Highly Cited
2003
Highly Cited
2003
Targeted doxorubicin-containing luteinizing hormone-releasing hormone analogue AN-152 inhibits the growth of doxorubicin-resistant MX-1 human breast cancers.
A. Bajo
,
A. Schally
,
G. Halmos
,
A. Nagy
Clinical Cancer Research
2003
Corpus ID: 11240155
PURPOSE The receptors for luteinizing hormone-releasing hormone receptor (LHRH-R) are found in >50% of human breast cancers…
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Highly Cited
2002
Highly Cited
2002
Antitumor effects of the cytotoxic luteinizing hormone-releasing hormone analog AN-152 on human endometrial and ovarian cancers xenografted into nude mice.
C. Gründker
,
P. Völker
,
+4 authors
G. Emons
American Journal of Obstetrics and Gynecology
2002
Corpus ID: 13315066
OBJECTIVE Most human endometrial and ovarian cancers express receptors for luteinizing hormone- releasing hormone. These…
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Highly Cited
2000
Highly Cited
2000
Receptor mediated antiproliferative effects of the cytotoxic LHRH agonist AN-152 in human ovarian and endometrial cancer cell lines.
S. Westphalen
,
Gaby Kotulla
,
+8 authors
Günter Emons
International Journal of Oncology
2000
Corpus ID: 28583504
Eighty percent of human ovarian and endometrial cancers express receptors for luteinizing hormone-releasing hormone (LHRH). These…
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1999
1999
Cytotoxic analogs of luteinizing hormone-releasing hormone bind with high affinity to human breast cancers.
G. Halmos
,
A. Nagy
,
N. Lamharzi
,
A. Schally
Cancer Letters
1999
Corpus ID: 29331184
Highly Cited
1997
Highly Cited
1997
Growth inhibition of human ovarian cancers by cytotoxic analogues of luteinizing hormone-releasing hormone.
M. Miyazaki
,
A. Nagy
,
+5 authors
P. Armatis
Journal of the National Cancer Institute
1997
Corpus ID: 11557517
BACKGROUND Receptors for luteinizing hormone-releasing hormone (LH-RH) are found in nearly 80% of human ovarian cancers. The…
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Highly Cited
1996
Highly Cited
1996
Cytotoxic analogs of luteinizing hormone-releasing hormone containing doxorubicin or 2-pyrrolinodoxorubicin, a derivative 500-1000 times more potent.
A. Nagy
,
A. Schally
,
+8 authors
J. Horváth
Proceedings of the National Academy of Sciences…
1996
Corpus ID: 8552206
Doxorubicin (DOX) and its daunosamine-modified derivative, 2-pyrrolino-DOX, which is 500-1000 times more active than DOX, were…
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