TARGETING OF LACTATE DEHYDROGENASE C, METHODS OF PREPARING SAME, AND METHODS OF USING SAME IN COMBINATION WITH ANTI-CANCER TREATMENTS
The present disclosure provides a therapeutic method comprised of targeting the tumor-associated antigen, Lactate Dehydrogenase C (LDHC), in LDHC-expressing cancers or tumors. This novel approach offers a highly specific cancer treatment with little or no off-target effects. Targeting LDHC with the use of silencing molecules increases tumor cell death by inducing excess DNA damage, and more importantly, can render breast tumor cells more responsive to non-specific, DNA damaging drugs and DNA damage repair inhibitors, such as platinum-based alkylating agents (e.g. cisplatin) and Poly ADP-Ribose Polymerase (PARP) inhibitors (e.g. olaparib). Targeting LDHC in tumor cells has the potential to specifically sensitize tumor cells to these drugs and/or inhibitors, leading to enhanced tumor cell killing and potentially minimizing side effects.
1 . A method of treating an LDHC-expressing cancer in a subject in need thereof, the method comprising administering to the subject an effective amount of a composition comprising an LDHC targeting molecule.
2 . The method of claim 1 , wherein the LDHC targeting molecule is administered or delivered to the subject via the use of a delivery system.
3 . The method of claim 1 , wherein the LDHC silencing molecule comprises short-interfering RNAs (siRNA).
4 . The method of claim 3 , wherein the siRNA is chemically modified to allow delivery of the naked siRNA into the subject's cells.
5 . The method of claim 1 , wherein the LDHC silencing molecule comprises vector-based short-hairpin RNAs (shRNA).
6 . The method of claim 1 , wherein the composition comprises an inhibitor, a nanobody, and/or antibody.
7 . The method of claim 6 , wherein the composition comprises at least one inhibitor.
8 . The method of claim 6 , wherein the composition comprises at least one nanobody.
9 . The method of claim 6 , wherein the inhibitor, antibody and/or nanobody is specific for the active site of LDHC or the substrate-binding site of LDHC.
10 . The method of claim 1 , wherein the delivery system comprises a DNA-scaffold based delivery system.
11 . The method of claim 1 , wherein the delivery system comprises lipid-based liposomes or lipoplexes.
12 . The method of claim 1 , wherein the delivery system comprises polymer-based nanoparticles or nanoplexes.
13 . The method of claim 12 , wherein the polymer-based nanoparticles or nanoplexes are complexed with polymers.
14 . The method of claim 1 , wherein the delivery system comprises nanostructures.
15 . The method of claim 1 , wherein the delivery system includes a biologically responsive delivery system.
16 . The method of claim 15 , wherein the biologically responsive delivery system comprises biosignal-responsive crosslinkers.
17 . The method of claim 1 , wherein the delivery system is modified with tumor homing peptides.
18 . The method of claim 1 , wherein the delivery system comprises cell- or tumor-derived extracellular vesicles/exosomes or their engineered forms.
19 . The method of claim 1 , wherein the LDHC silencing molecule is administered to a subject with LDHC-expressing cancer, in an amount effective to partially or fully degrade the LDHC mRNA.
20 . The method of claim 1 , wherein the LDHC silencing molecule is administered to a subject with LDHC-expressing cancer, in an amount effective to reduce or eliminate the production of LDHC protein or LDHC antigen in tumors or cancer cells.
21 . A method of preventing the progression, decreasing incidence of, and/or decreasing severity of an LDHC-expressing tumor in a subject in need thereof, the method comprising administering to the subject a composition comprising an effective amount of LDHC targeting molecules.
22 . The method of claim 21 , wherein the subject is human.
23 . The method of claim 21 , wherein the composition is administered systemically and/or locally.
24 . The method of claim 21 , wherein the composition comprises a DNA damaging drug and/or DNA damage repair inhibitor.