Use for PAI-1 inhibitor
Provided is a novel use of a plasminogen activator inhibitor-1 inhibitor (PAI-1 inhibitor) that is used as an active ingredient of an agent for controlling a tumor stem cell, an agent for enhancing the antitumor effect of an antitumor agent, an agent for tumor chemotherapy, a stem-cell protecting drug, or a hematopoietic disorder improving agent.
1. A method for treating a tumor in a patient, the method comprising:
(i) administering a compound having PAI-1 inhibitory activity to a patient having a tumor, wherein said tumor is selected from the group consisting of chronic myelogenous leukemia, lymphoma, and ovarian cancer, and wherein the compound is represented by Formula (I) or a pharmacologically acceptable salt thereof:
wherein
either R 1 or R 2 is hydrogen, and the other is halogen;
X is vinylene (—CH═CH—);
A is a group represented by Formula (I-1):
in Formula (I-1), q is an integer of 1;
both of R 3 and R 4 are hydrogen;
T is a single bond;
D is phenyl, quinolyl, isoquinolyl, or furyl;
L is a single bond, —CONH—, or alkyleneoxyalkylene-CONH—; and
B is COOR 9 , wherein R 9 is hydrogen or a group converted to hydrogen in vivo,
wherein the compound does not show an antitumor effect in vivo when the compound is administered alone, and
(ii) administering an antitumor agent, wherein the antitumor agent has anti-tumor activity against one or more of chronic myelogenous leukemia, lymphoma, and ovarian cancer.
2. The method according to claim 1 , wherein
B is located at the ortho position of the benzene ring to which imino is bound, and R 9 is hydrogen in Formula (I).
3. The method according to claim 1 , wherein the compound having PAI-1 inhibitory activity is at least one member selected from the group consisting of
2-[(biphenyl-3-ylcarbonyl)amino]-5-chlorobenzoic acid,
sodium 5-chloro-2-({[3-(quinolin-8-yl)phenyl]carbonyl}amino)benzoate,
5-chloro-2-{[{[3-(furan-3-yl)phenyl]amino}(oxo)acetyl]amino}benzoic acid, and
5-chloro-2-{[(2-{[3-(furan-2-yl)phenyl]amino}-2-oxoethoxy)acetyl]amino}benzoic acid.
4. The method according to claim 1 , wherein the antitumor agent is at least one member selected from the group consisting of antimetabolites, microtubule inhibitors, antitumor antibiotics, topoisomerase inhibitors, platinum-based drugs, alkylating agents, hormone-like drugs, molecular targeted drugs, antibody drugs, cytokines, and non-specific immunostimulants.
5. The method according to claim 1 , wherein D is quinolyl.