Klaus Nickisch

No ORCID on file · 7 papers in corpus
review 2026
Cancer letters ·doi:10.1016/j.canlet.2026.218845

Endometriosis is a chronic, estrogen-dependent inflammatory disease that, despite its benign histology, displays several cancer-relevant features, including clonal expansion, somatic alteration-associated lesion evolution, tissue invasion, …

review 2020
Hormone molecular biology and clinical investigation ·doi:10.1515/hmbci-2020-0013

The different etiopathogenetic mechanisms and the diversity of clinical features of endometriosis has not yet allowed to identify a causal pharmacological monotherapy satisfying the unresolved medical needs in this important female disease.…

lab-animal 2019
Scientific reports ·doi:10.1038/s41598-019-53467-w

Uterine fibroids (UFs) are associated with irregular or excessive uterine bleeding, pelvic pain or pressure, or infertility. Ovarian steroid hormones support the growth and maintenance of UFs. Ulipristal acetate (UPA) a selective progestero…

lab-animal 2018
Steroids ·doi:10.1016/j.steroids.2018.07.010

An effort with the goal of discovering single-dose, long-lasting (>6 months) injectable contraceptives began using levonorgestrel (LNG)-17-β esters linked to a sulfonamide function purposed as human carbonic anhydrase II (hCA 2) ligands. On…

lab-animal 2016
Oncotarget ·doi:10.18632/oncotarget.7516

Endometriosis is a chronic estrogen-dependent disease that occurs in approximately 10% of reproductive age women. Baboons offer a clear benefit for studying the initiation and progression of endometriosis since baboon is very close to human…

lab-animal 2013
Steroids ·doi:10.1016/j.steroids.2013.04.003

Progesterone receptor (PR) plays a key role in reproductive functions, and compounds that inhibit progesterone action (antiprogestins) have potential use in the treatment of estrogen- and progesterone-dependent diseases, including uterine l…

lab-animal 2013
Steroids ·doi:10.1016/j.steroids.2012.09.010

A series of antiprogestins have been synthesized by partially fluorinating the steroid molecule in positions relevant for receptor binding. By introducing fluorine at the exo-methylene of the 17 spirofuran ring, we obtained partial agonists…