Assays for non-apoptotic cell death and uses thereof
View Patent ↗The invention relates to methods for identifying agents, which induce oxidative cell death in a tumor cell. The invention further relates to methods for identifying tumor cells, which are sensitive to agents that induce oxidative cell death. The invention also relates to methods for identifying subjects who are suffering from tumors, which are sensitive to agents that induce oxidative cell death.
1. A method for identifying an agent, which induces RAS-RAF-MEK-dependent oxidative non-apoptotic cell death of a tumor cell, the method comprising:
(a) detecting increasing VDAC level in the tumor cell, wherein the VDAC is selected from the group consisting of VDAC1, VDAC2, VDAC3, and combinations thereof,
(b) contacting the tumor cell with the agent, and
(c) determining whether the tumor cell dies via oxidative non-apoptotic cell death, comprising:
(I) detecting an increased level of oxidative species in the tumor cell; and
(II) identifying one or more of: (i) a lack of caspase 3 cleavage or activation; (ii) a lack of cytochrome C release; (iii) a lack of PARP cleavage or activation; (iv) a lack of Annexin V staining; (v) lack of alterations in chromatin morphology; (vi) a lack of nuclear DNA laddering; (vii) a lack of TUNEL staining of nuclear DNA; and (viii) a lack of depletion of ATP levels,
wherein if the tumor cell dies via oxidative nonapoptotic cell death, then the agent induces RAS-RAF-MEK-dependent oxidative non-apoptotic cell death.
2. The method according to claim 1 , further comprising (d) determining whether mitochondrial morphology of the tumor cell is altered, wherein altered mitochondrial morphology of the tumor cell is further indicative that the agent induced the oxidative non-apoptotic cell death.
3. The method according to claim 1 , wherein the oxidative non-apoptotic cell death is iron-dependent.
4. The method according to claim 1 , wherein step (c)(II) comprises identifying all of: (i) a lack of caspase 3 cleavage or activation; (ii) a lack of cytochrome C release; (iii) a lack of PARP cleavage or activation; (iv) a lack of Annexin V staining; (v) lack of alterations in chromatin morphology; (vi) a lack of nuclear DNA laddering; (vii) a lack of TUNEL staining of nuclear DNA; and (viii) a lack of depletion of ATP levels.
5. A method for identifying a first agent, which induces RAS-RAF-MEK-dependent oxidative non-apoptotic cell death of a tumor cell, the method comprising:
(a) detecting increasing VDAC level in the tumor cell, wherein the VDAC is selected from the group consisting of VDAC1, VDAC2, VDAC3, and combinations thereof,
(b) contacting the tumor cell with the first agent in the presence and absence of a second agent selected from the group consisting of an iron chelator, an anti-oxidant, and an inhibitor of mitochondria-generated oxidative species, and
(c) determining whether the tumor cell dies via oxidative non-apoptotic cell death in the absence of the second agent, comprising:
(I) detecting an increased level of oxidative species in the tumor cell; and
(II) identifying one or more of: (i) a lack of caspase 3 cleavage or activation; (ii) a lack of cytochrome C release; (iii) a lack of PARP cleavage or activation; (iv) a lack of Annexin V staining; (v) lack of alterations in chromatin morphology; (vi) a lack of nuclear DNA laddering; (vii) a lack of TUNEL staining of nuclear DNA; and (viii) a lack of depletion of ATP levels,
wherein if the tumor cell dies via oxidative nonapoptotic cell death in the absence of the second agent, but is viable in the presence of the second agent, then the first agent induces RAS-RAF-MEK-dependent oxidative non-apoptotic cell death.
6. The method according to claim 5 , wherein step (c)(II) comprises identifying all of: (i) a lack of caspase 3 cleavage or activation; (ii) a lack of cytochrome C release; (iii) a lack of PARP cleavage or activation; (iv) a lack of Annexin V staining; (v) lack of alterations in chromatin morphology; (vi) a lack of nuclear DNA laddering; (vii) a lack of TUNEL staining of nuclear DNA; and (viii) a lack of depletion of ATP levels.
7. The method according to claim 2 , wherein the tumor cell expresses a fluorescently labeled VDAC protein, and the method further comprises:
(d) measuring the fluorescent signal due to the fluorescently labeled VDAC protein,
wherein if the tumor cell dies via oxidative nonapoptotic cell death, and if the fluorescence due to the fluorescently labeled VDAC protein decreases, then the agent induces RAS-RAF-MEK-dependent non-apoptotic oxidative cell death.
8. The method according to claim 2 , wherein the tumor cell expresses a fluorescence resonance energy transfer (FRET) system comprising a VDAC protein with two different fluorescent labels, wherein the labeled VDAC protein exhibits fluorescent emission at a first and second wavelength when VDAC is open, or a first, second and third (FRET) wavelength when VDAC is closed;, and the method further comprises:
(d) measuring a fluorescent signal due to the fluorescently labeled VDAC protein,
wherein if the tumor cell dies via oxidative nonapoptotic cell death, and if the fluorescence due to FRET in the labeled VDAC protein decreases, then the agent induces RAS-RAF-MEK-dependent non-apoptotic oxidative cell death.
9. The method according to claim 2 , further comprising:
(d) providing a non-tumor cell that is syngeneic to the tumor cell, and
(e) measuring a level of VDAC in the non-tumor cell,
wherein if the level of VDAC in the tumor cell is increased compared to the VDAC level in the syngeneic non-tumor cell and if the tumor cell dies via oxidative non-apoptotic cell death, then the tumor cell is susceptible to the agent which induces RAS-RAF-MEK-dependent non-apoptotic oxidative cell death.
10. The method according to claim 9 , wherein VDAC protein level is measured in step (e).
11. The method according to claim 9 , wherein VDAC mRNA level is measured in step (e).
12. The method according to claim 9 , wherein the tumor cell and the syngeneic cell are derived from a subject having a tumor.