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Volledige samenvatting Algemene en Experimentele Oncologie 2025/2026

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Dit document is een samenvatting van het volledige vak Algemene en Experimentele Oncologie uit de 3de bachelor biomedische wetenschappen in UA, en bevat zowel alle informatie/foto's uit de slides als alle leerstof die besproken werd in de les. Zelf behaalde ik een 17/20 op het examen.

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INHOUDSOPGAVE

1. CELDELING ALS MOTOR VAN ONTWIKKELING, GROEI EN WEEFSELHOMEOSTASE ........ 12

2. NEOPLASTISCHE GROEI ............................................................................................. 12

3. INVASIEF EN METASTATISCH GEDRAG ........................................................................ 13

4. SELECTIE VAN TUMORCELLEN .................................................................................... 14

DE "HALLMARKS OF CANCER" .............................................................................................. 14

1) ZELFVOORZIENEND IN GROEIFACTOREN .................................................................................... 15

2) ONGEVOELIG VOOR GROEIREMMENDE SIGNALEN ........................................................................ 15

3) VERMIJDEN VAN CELDOOD (APOPTOSE) .................................................................................... 15

4) ONBEPERKTE CELDELING (IMMORTALISATIE) ............................................................................... 16

5) INDUCTIE VAN ANGIOGENESE ................................................................................................. 16

6) ACTIVATIE VAN INVASIE EN METASTASERING ............................................................................... 17

AANVULLENDE HALLMARKS (2011: +4 KENMERKEN)................................................................... 17

7) GENOMISCHE INSTABILITEIT EN MUTATIES .................................................................................. 17

8) TUMOR-BEVORDERENDE INFLAMMATIE ..................................................................................... 17

9) HERPROGRAMMEREN VAN ENERGIEMETABOLISME ....................................................................... 18

10) ONTWIJKEN VAN HET IMMUUNSYSTEEM ................................................................................... 18

AANVULLENDE HALLMARKS (2022: +4 KENMERKEN)................................................................... 18

11) FENOTYPISCHE PLASTICITEIT ONTSLUITEN ................................................................................ 18

12) EPIGENETISCHE HERPROGRAMMERING ................................................................................... 18

13) BELANG VAN HET MICROBIOOM ............................................................................................. 19

14) SENESCENTE CELLEN.......................................................................................................... 19

BELANGRIJK: TUMOR MICRO-OMGEVING ....................................................................... 19

BELANGRIJK: ONTWIKKELEN VAN DOELGERICHTE ANTI-KANKERTHERAPIEËN ................ 19

5. HOE MANIFESTEERT KANKER ZICH IN EEN PATIËNT? ................................................... 19


1

,6. TUMORCLASSIFICATIE ............................................................................................... 20

HERHALING: HALLMARKS OF CANCER (EERSTE 10) ......................................................... 22

RECENT TOEGEVOEGDE 4 KENMERKEN (14 HALLMARKS TOTAAL):................................................... 22

2 GROTE CATEGORIEËN VAN GENEN .............................................................................. 22

1. ONCOGENEN ................................................................................................................ 22

MECHANISMEN VAN VIRALE ONCOGENESE .................................................................................... 23

GENETISCHE MECHANISMEN DIE LEIDEN TOT CONSTITUTIEVE ACTIVATIE VAN ONCOGENEN BIJ DE MENS ....... 24

2. TUMORSUPPRESSORGENEN (TSG) ..................................................................................... 27

"TWO-HIT"-HYPOTHESE VAN KNUDSON ........................................................................................ 27

TUMORSUPPRESSORGENEN ....................................................................................................... 30

KANKER ALS ZIEKTE VAN DE CELCYCLUS ....................................................................... 30

1. APOPTOSE IN CARCINOGENESE EN KANKERBEHANDELING ........................................ 31

APOPTOSE = GEPROGRAMMEERDE CELDOOD ............................................................................ 31


VERSTORING APOPTOSE = CENTRALE STAP IN TUMORALE TRANSFORMATIE! ....................................... 31


A) APOPTOSE VS. NECROSE ....................................................................................................... 31

B) MORFOLOGISCHE KENMERKEN VAN APOPTOSE ........................................................................... 32

C) APOPTOSE VERLOOPT IN 3 FASEN ............................................................................................ 32

D) DE EXECUTIEFASE VAN APOPTOSE ............................................................................................ 33

E) DE INTRINSIEKE OF MITOCHONDRIALE PATHWAY .......................................................................... 33

F) DE EXTRINSIEKE OF 'DEATH RECEPTOR' PATHWAY ......................................................................... 35

G) DE APOPTOSE-CASCADE ALS DOELWIT VOOR ANTIKANKERTHERAPIE ................................................ 35

2. P53: BEWAKER VAN HET GENOOM ....................................................................................... 36

A) HISTORIEK VAN P53 .............................................................................................................. 36

B) STRUCTUUR VAN WILD TYPE EN GEMUTEERD P53 ......................................................................... 36

C) REGELING VAN P53-CONCENTRATIE EN -ACTIVITEIT IN BASALE OMSTANDIGHEDEN .............................. 37

D) REGELING VAN P53-CONCENTRATIE EN -ACTIVITEIT IN ABNORMALE OMSTANDIGHEDEN ....................... 37

2

,E) CELLULAIRE EFFECTEN VAN VERHOOGDE P53-ACTIVITEIT .............................................................. 37

F) P53 ALS AANGRIJPINGSPUNT VOOR MOLECULAIRE ANTIKANKERTHERAPIE .......................................... 39

1. INTRODUCTIE ............................................................................................................ 40

RADIOTHERAPIE WERKT! ...................................................................................................... 40

IRIDIUM NETWERK ANTWERPEN ............................................................................................ 40

MULTIDISCIPLINAIR CONSULT (MOC) ..................................................................................... 40

DOEL VAN DE BEHANDELING ................................................................................................. 40

2. RADIOTHERAPIE IN DE PRAKTIJK................................................................................. 40

WAT IS RADIOTHERAPIE? ..................................................................................................... 40

ATOOMSTRUCTUUR & IONISATIE ............................................................................................ 41

SOORTEN STRALING ........................................................................................................... 41

EENHEID VAN STRALING ...................................................................................................... 41

TUMOR VERDUBBELINGSTIJD................................................................................................. 41


TUMORBIOLOGIE ............................................................................................................... 42

HOE WERKT RADIOTHERAPIE? ............................................................................................... 42

EFFECT VAN STRALING OP WEEFSELS ...................................................................................... 42

FRACTIONERING ................................................................................................................ 43

DOEL VAN RADIOTHERAPIE ................................................................................................... 43

THERAPEUTISCHE BREEDTE .................................................................................................. 43

RADIORESISTENTIE ............................................................................................................ 43

POGINGEN TOT VERBETERING VAN EFFECTIVITEIT ....................................................................... 43

COMBINATIEBEHANDELINGEN .............................................................................................. 44

WIE KOMT IN AANMERKING VOOR RADIOTHERAPIE? .................................................................... 44

HOE LANG BESTAAT RADIOTHERAPIE? ..................................................................................... 44

BRACHYTHERAPIE .............................................................................................................. 44

WAT HEB JE NODIG VOOR MODERNE RADIOTHERAPIE................................................................... 45

3

, MACHINERIE........................................................................................................................... 45

MENSEN ................................................................................................................................ 45

CT/MRI DOSIMETRIE & BEELDVORMING .................................................................................. 45

TREATMENT PLANNING SYSTEM............................................................................................. 45

BEELDGESTUURDE PLANNING ............................................................................................... 46

LINEAIRE VERSNELLER: TECHNIEK .......................................................................................... 46

3. BIJWERKINGEN RADIOTHERAPIE ................................................................................ 46

INDELING: ACUUT VS. LAAT................................................................................................... 46

ACUTE BIJWERKINGEN ........................................................................................................ 46

LATE BIJWERKINGEN ........................................................................................................... 47

4. MODERNE RADIOTHERAPIE ........................................................................................ 47

ONTWIKKELING IN TECHNIEK ................................................................................................ 47

WAAROM NIEUWE TECHNIEKEN NODIG? .................................................................................. 47

WAARDOOR WERD HET MOGELIJK? ........................................................................................ 47

WAT IS BELANGRIJK BIJ DE NIEUWE TECHNIEKEN? ....................................................................... 47


KLASSIEKE RADIOTHERAPIE .................................................................................................. 47


IMRT: INTENSITEITSGEMODULEERDE RADIOTHERAPIE ................................................................. 48

4D: ADEMHALINGSGECONTROLEERDE RT ................................................................................ 48

IMAGE GUIDED RADIOTHERAPIE (IGRT) ................................................................................... 48

5. NIEUWE ONTWIKKELINGEN ........................................................................................ 48

RECENTE ONTWIKKELINGEN (OVERZICHT) ................................................................................ 48

GOUDMARKERS (VISICOILS®) ................................................................................................ 48

STEREOTACTISCHE RADIOCHIRURGIE EN RADIOTHERAPIE ............................................................ 48

SBRT WERVELMETASTASEN ................................................................................................. 49

MRI-GELEIDE RADIOTHERAPIE .............................................................................................. 49

PROTON/HADRON THERAPIE ................................................................................................ 49

4

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