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ONCOLOGIA MOLECULARONCOLOGIA MOLECULAR
Maestría en Biología
Molecular Médica –2008
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¿¿QUE ES EL CANCER?QUE ES EL CANCER?
1)1) ProliferaciProliferacióón ilimitadan ilimitada2)2) Capacidad de dar metCapacidad de dar metáástasisstasis
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Normal cell division: enough to replaceMBMM 2008
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Excessive proliferation …….MBMM 2008
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Tumours attract a blood supply
By secreting tumour angiogenesis factors
(Misuse of a normal mechanism) MBMM 2008
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Metastasis: formation of secondary tumours
NB: This requires survival without anchorageMBMM 2008
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¿¿COMO SE PRODUCE EL COMO SE PRODUCE EL CANCER?CANCER?
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ONCOGENES
Maestría en Biología Molecular Médica –2008
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Maestría en Biología Molecular Médica –
Dr. José Mordoh 2008
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Maestría en Biología Molecular Médica –
Dr. José Mordoh 2008
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Maestría en Biología Molecular Médica –
Dr. José Mordoh 2008
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Maestría en Biología Molecular Médica –
Dr. José Mordoh 2008
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• PROTO-ONCOGENE = GEN NORMAL• SUSCEPTIBLE DE TRANSFORMACIÓN
• ONCOGENE = GEN MUTADO
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Maestría en Biología Molecular Médica –
Dr. José Mordoh 2008
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ONCOGENES PROTOTIPICOS= PROPIEDADESFunción Oncogene Propiedades
Tirosina-Quinasas Integrales de V-ERB B EGFR-SIMILMembrana HER 2-NEU RECEPTORTirosina-Quinasas Asociadas a V-SRC TRANSDUCCIONMembrana V-ABLSerina-Treonina Quinasas V-MOS
RAF TRANSDUCCIONFamilia Factores Crecimiento V-SIS PDGFFamilia Ras V-H-RAS TRANSDUCCION
V-K-RASN-RAS
Familia Proteínas Nucleares V-MYC UNION DNAN-MYCV-MYBV-FOSV-JUN
Varios INT-1
Maestría en Biología Molecular Médica –
Dr. José Mordoh 2008
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Mecanismos de Transformación de Proto-oncogene a oncogene
1. Translocación2. Amplificación3. Inserción Viral4. Mutagénesis
Maestría en Biología Molecular Médica –
Dr. José Mordoh 2008
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Maestría en Biología Molecular Médica –
Dr. José Mordoh 2008
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Maestría en Biología Molecular Médica –
Dr. José Mordoh 2008
Figure 1. The Translocation of t(9;22)(q34;q11) in CML. The Philadelphia (Ph) chromosome is a shortenedchromosome 22 that results from the translocation of 3' (toward the telomere) ABL segments on chromosome 9 to5' BCR segments on chromosome 22. Breakpoints (arrowheads) on the ABL gene are located 5' (toward thecentromere) of exon a2 in most cases. Various breakpoint locations have been identified along the BCR gene onchromosome 22. Depending on which breakpoints are involved, different-sized segments from BCR are fused withthe 3' sequences of the ABL gene. This results in fusion messenger RNA molecules (e1a2, b2a2, b3a2, ande19a2) of different lengths that are transcribed into chimeric protein products (p190, p210, and p230) with variable molecular weights and presumably variable function. The abbreviation m-bcr denotes minor breakpoint cluster region, M-bcr major breakpoint cluster region, and µ-bcr a third breakpoint location in the BCR gene that isdownstream from the M-bcr region between exons e19 and e20.
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Figure 2. Functional Domains of p160BCR, p145ABL, and p210BCR–ABL. Important functional domains of the BCR and ABL gene products as well as of the different fusion-protein products are shown. Breakpoints are indicated by arrowheads (see Table 2 and the text fordetails). N denotes N-terminal amino acid sequence, C C-terminal amino acid sequence, Ser–thr serine–threonine, GDP guanosine diphosphate, GTP guanosine triphosphate, GEF GDP–GTP exchange factor, DBL diffuse B-cell lymphoma oncogene, RAC a RAS-like GTPase, GAP guanosine triphosphatase–activating function, and SH SRC homology domain.
Maestría en Biología Molecular Médica –
Dr. José Mordoh 2008
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Mecanismos de Transformación de Proto-oncogene a oncogene
1. Translocación2. Amplificación3. Inserción Viral4. Mutagénesis
Maestría en Biología Molecular Médica –
Dr. José Mordoh 2008
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Maestría en Biología Molecular Médica –
Dr. José Mordoh 2008
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Mecanismos de Transformación de Proto-oncogene a oncogene
1. Translocación2. Amplificación3. Inserción Viral4. Mutagénesis
Maestría en Biología Molecular Médica –
Dr. José Mordoh 2008
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Maestría en Biología Molecular Médica –
Dr. José Mordoh 2008
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Maestría en Biología Molecular Médica –
Dr. José Mordoh 2008
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Mecanismos de Transformación de Proto-oncogene a oncogene
1. Translocación2. Amplificación3. Inserción Viral4. Mutagénesis
Maestría en Biología Molecular Médica –
Dr. José Mordoh 2008
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Maestría en Biología Molecular Médica –
Dr. José Mordoh 2008
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GENES SUPRESORESGENES SUPRESORES
Dr. Jose MordohMaestria en Biologia Molecular
Medica 2008
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Maestría en Biología Molecular Médica –
Dr. José Mordoh 2008
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ENFERMEDAD GENÉTICA RECESIVAHIPÓTESIS DE KNUDSON
Mutación somáticaMutación germinal
Fenotipo normal
Fenotipo neoplásico
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Maestría en Biología Molecular Médica –
Dr. José Mordoh 2008
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Maestría en Biología Molecular Médica –
Dr. José Mordoh 2008
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Figure 2. Functional and Pathogenic Properties of APC
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CADHERINS AND THEIR ROLEIN CANCER METASTASIS
MBMM 2004
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Cadherin is composed of a single protein chain thatfolds into a series of domains. On the outside of thecell, there are five compact domains. Calcium ions, shown here as blue spheres, bind atthe junction between the domains. They providestability and are essential for proper adhesivefunction. The adhesive site is in the uppermostdomain and relies on a key tryptophan amino acid, shown here in red. Inside the cell, there is a smalldomain that interacts with catenins and otherproteins that bind to the cytoskeleton. This regionis shown as a schematic here, with the cellmembrane in green. Coordinates for theextracellular region were taken from entry 1l3wat the Protein Data Bank (www.pdb.org).
MBMM 2004
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HIPOTESIS DE LA VIGILANCIA
INMUNOLÓGICA
RATONES KNOCK – OUT PARA RECEPTOR DE IFN-γ Y STAT
GENERAN ESPONTÁNEAMENTE TUMORES
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Las “tres E” de la inmunoedición
Nature Immunol 2002; 3:991.
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METASTASIS
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MODELS OF THE METASTATIC CASCADE
MBMM 2008
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Proteases in metastasis• Urokinase-like plasminogen activator
– Serine protease– Attached to invasive cell surface.– Activates tissue plasminogen to plasmin, which is not specific.
• Matrix metalloproteinases– Zinc metalloproteinase– >27 family members– Important in tissue remodeling
• Cathepsins– cysteine proteases (B,S,L,O,W,F,C,H,Z)– Aspartic proteases (D)– Lysosomal, released to ECM, or degrades MMP framents– B, D and L important in colon, prostate and breast cancer
progression
MBMM 2008
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Cadherins extend from the surface of the cell and attach to cadherinson a neighboring cell. Here, a portion of an adherens junction is shown, with cadherin molecules in red. The two cell membranes are shown in lightgreen, and the cadherin molecules are linked in the space between the twocells. Just inside each cell, catenin molecules (in green) link the cadherinsto actin filaments (in blue).
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PATOLOGIA MOLECULAR DE LA METASTASIS
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Diagnóstico molecular de diseminación linfática
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Lymph node involvement is indicative of poor prognosis in severalcancer types, because it indicates clear evidence of metastaticdisease.
A subset of patients with histologically node negative disease willdevelop metastatic disease with subsequent reduced survival.
Using molecular staging techniques micrometastases are definedas single disseminated tumor cells or small clusters of neoplasticcells which can only be detected by immunohistochemicaltechniques or assays based on PCR
With these techniques, lymph-node micrometastases can be detected in up to 40% of nodenegative patients with breast cancer, and non-small-celllung cancer
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Principio de ganglio centinela
The development of the dynamic technique of intraoperative lymphaticmapping in the 1990s resulted in general acceptance of the sentinel nodeconcept.
This hypothesis of sequential tumour dissemination seems to be validaccording to numerous studies of sentinel node biopsy with confirmatoryregional lymph node dissection.
Sentinel node biopsy is a minimallyinvasive technique to select patientswith occult lymph node metastaseswho may benefit from further regional or systemic therapy.
The sentinel node is the first lymphnode reached by metastasising cellsfrom a primary tumour.
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The surgeon injects a small dose of radioactive tracer(technetium-99) into the breast in the region of thepatient’s tumor.
Next, the surgeon will wait for the technetium-99 totravel from the tumor region to the sentinel lymphnode(s). Depending on the protocol followed, thesurgeon usually waits between 45 minutes to 8 hoursafter injection before performing the biopsy.
At some point during the procedure, a small amount ofblue dye (isosulfan blue) will also be injected near thearea of the tumor.
Once the technetium-99 tracer and dye have reachedthe nodes, the surgeon will scan the area with anelectric, hand-held gamma ray counter attached to a small probe which the surgeon traces over the axilla oringle to locate the sentinel node(s).
Procedimiento de ganglio centinela
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The surgeon will make a small incision (usually one-half inch) and remove the sentinel node(s) for a pathologist to examine under a microscope. The blue dye provides additional visual confirmation of thesentinel node’s location during surgical removal.
The sentinel lymph nodes will be classified as negative (no cancer), positive(contain cancer), or indeterminate. However, this preliminary report is followedby close examination and the final pathology report.
If the sentinel node is determined to be cancerous while the patient is still in surgery, the surgeon will usually remove additional lymph nodes in the axilla.
However, the final pathology report is not available until after the surgery has been completed, and patients should schedule a follow-up visit with thesurgeon to discuss the final report.
Sometimes, the final report indicates a positive (cancerous) sentinel node thatwas not seen on preliminary review. If this occurs, then additional surgery may be necessary to remove more nodes for examination.
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MBMM 2004MBMM 2008
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Metastatic adenocarcinoma is seen in a lymph node here.It is common for carcinomas to metastasize to lymph nodes.MBMM 2008